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Showing posts with label clinical trials. Show all posts
Showing posts with label clinical trials. Show all posts

Friday, December 6, 2019

Sponsor Key Performance Indicators - Part 1

Sponsor Performance KPI - Part 1

Sponsors are the key stakeholders in clinical trials. It is important to measure the performance of sponsors to understand the trends in the industry and market. Metrics such as studies registered, studies completed, study results posted, collaboration and study completion duration can be key performance indicators from study conduct perspective. We can gain competitive intelligence about competitor sponsors or find opportunities to collaborate with potential partners. The possibilities are endless. 
Let's see who were top Industry sponsors in terms of studies completed in 2018 ranked by number of completed studies. 

There are 4,017 studies completed by industry sponsors in 2018. Novartis is leading the board with 114 studies completed in 2018, followed by GSK and Pfizer with 96 and 92 studies respectively. The chart also shows the number of results posted by those sponsors in 2018. There may be studies completed in 2018 for which the results are not posted yet, but I am not aware of any requirements for posting results. Another metric is the ration of completed studies to the studies with posted results. There should be a linear relationship since more completed studies would mean more posted results. To just verify that, let's create a scatter plot. There is a strong linear relationship. The R-square value is pretty high. See the plot below with a fitted line. It may be interesting to look at sponsors with very low ratio.
  

Now, let's take a look at what's going on with non-industry sponsors in the same year 2018.

NIH, Mayo clinic and Duke University are the top 3 performers. 
The studies completed numbers are comparable  but the posted results and the ratio is very low when compared to sponsors from industry segment. The slope is 0.13 as compared to 0.3 for industry sponsors. So, we see that industry sponsors are posting more results. 
   
We can see that the industry sponsors(blue) have higher posted results for same levels of completed studies as compared to the non-industry sponsors(red).
I am really trying to think why non-industry sponsors have low results postings than industry sponsors. 
Every study is required to submit the results, generally no later than 12 months of completion.
The clinicaltrials.gov explains what all is included in the results and also mentions few valid reasons when the results are not submitted:
https://clinicaltrials.gov/ct2/about-site/results#DisplayOfResults 

Good news!!! I have recreated sponsor analytics using flexdashboards and plotly R so that you all can interact instead of viewing static jpeg images. The charts are very interactive and you can view individual data points. However, in the analysis, I have only included sponsors that have completed at least 10 studies, to reduce the number of data points as well as the skewness caused by them since there were a large numbers of sponsors within that range. I hope you would enjoy that.
Link to Dashboard:
http://rpubs.com/kalehdoo/SponsorDashboard

Summary -There are a total of 2234 sponsors who have completed at least 10 studies in the past out of which there are 647 (29%) sponsors from Industry and the remaining 1587 (71%) from non-industry.
Non-industry sponsors are further classified into Academic and Hospital based on their names (this may not be 100% correct and you may notice some sponsors classified incorrectly).
Keep reading!!!


    

Friday, November 15, 2019

Clinical Study Activity Per Capita


Study Activity Dashboard

In this post, we will try to understand the clinical study activities across the globe. We will gather some inputs like population, GDP and health spending as % of GDP. Then we compare different countries by their involvement in clinical studies. The clinical study activity is based on the clinical site in that country for a particular study. It is important to keep in mind that those clinical sites or facilities may or may not have enrolled any participants. Also, the demographics data is for the year 2017 and we are considering all the clinical studies registered in the USA clinicaltrials.gov as of Aug 2019. Keeping all that in mind, we will try to get a sense of overall study activity and compare them for different countries. We will also look at the study activity from region level. So, just sit back and relax.
Figure 1.1
Figure 1.1 shows study activity per 100 K population of a country. Denmark tops the list with the highest number of studies per 100 K population. This is not the complete list and I have tried to display maximum I could fit in a picture. You would notice that there are countries with very small population and hence they have got a high activity per capita. Also, there are few countries with very large populations and have got a low ratio.

In figure 1.2 above, the countries are categorized under geographic region. It also shows the percentage share of the population and number of studies. The dashboard allows to drill down on a region and see the details by country. 
We will look at the study activity based on the GDP and health spending as % of GDP of countries in next post.
Keep thinking till next time. 

Wednesday, September 11, 2019

Clinical Intelligence Analytics - Sponsor Trends

Sponsor Trends Dashboard

In the last post here, we gained some insights into top performing sponsors and overall trend. In this post, we will look further deep into how the sponsor participation has changed in last few years. The Sponsor Trends Dashboard (figure 6.1) can answer some interesting questions and see what's going on in the clinical trials industry.

Figure 6.1
Here, we will try to analyze the insights gained from Sponsor Trends Dashboard in Figure 6.1 above. 
1. What type of study Sponsors have the highest or lowest share in study registration, and how has that changed over the last few years?
The chart in Quadrant 2 tells us about the share of studies by different types of sponsors. Clearly, Universities have the highest share and has maintained a steep rise in the last few years. The share has increased from 40% in 2005 to 50% in last 2 years. These Universities could be public or private, funded or not-funded but we do not have that information available as of now. 
Hospitals have also performed well in registering the studies. The share of studies registered by Hospitals have almost doubled since 2005. On the other hand, the share of Industry sponsored studies has declined consistently and it has reduced to just 17% now which was 37% in 2008. The share does not indicate if the segment has really grown or declined. The share of one segment, Universities for example,  could rise because other segments have declined. To see the trend, read the next question below.

2. Which type of sponsors have shown growth in study activity?
The chart in Quadrant 1 shows how the registered studies by different categories or types of sponsors have grown over the period.
The studies registered by Universities have grown at a continuous and rapid pace. Until 2008, the Industry segment and Universities were overlapping but after that the Universities completely outpaced the Industry Sponsors. The growth in studies registered by Industry sponsors has remained almost flat but Hospitals maintained a steady growth until 2016 after which the growth is negligible. 

3. How has the total numbers of sponsors changed over the past few years?
In the above 2 charts in Quadrants 1 and 2, we looked at the trend of the studies registered by sponsors but now in this chart on quadrant 3, we will look at the trend of actual number of sponsors.
The overall trend shows that the total number of primary sponsors who registered their studies has grown consistently. All 3 important categories, Universities, Industry Sponsors and Hospitals have grown consistently. All 3 types of sponsors have increased almost 2 times of 2008 levels.

4. Has the participation of sponsors from industry has increased?
The chart in quadrant 4 shows the participation trend over the period. Industry participation means that either the study is sponsored by a sponsor from industry or at least one of the collaborators is an industry sponsor. 
The chart shows that the industry participation has declined and reduced to just 22% from upper 40s in 2008. Between 2005 and 2008, the share of studies having industry participation remained in upper 40s but started declining consistently after 2008. However, it is not clear from this chart if the studies with industry participation has decreased or the studies without industry participation has increased. To figure that out, let's take a look at the trend chart that shows the number of studies with or without industry participation over the period of time.
Figure 6.2

The trend in chart (figure 6.2) shows that the number of studies where there is industry participation has remained nearly constant but the studies without any industry participation has increased from 6K levels in 2005 to 24K in 2018, which is four times growth.
As a food for thought, how do you think clinical research industry can increase the collaboration for the larger benefit to the whole community?
Do post your questions and comments.
Keep thinking!

Source data extracted from: https://aact.ctti-clinicaltrials.org 

Saturday, September 7, 2019

Clinical Intelligence Analytics - Primary Sponsor

Primary Sponsor Dashboard

Primary Sponsor dashboard (Figure 5.1) provides us insights into the study activities by primary or lead study sponsors. Primary sponsor is an important stakeholder in the clinical trials that has the primary responsibility of initiating, study design and study conduct. In simple terms, we can say that the primary sponsor is the owner of the clinical study. The sponsor can be an individual, a company or an institution, and they can be from industry (commercial) like pharmaceutical or Biotech companies or public non-industry (non-commercial) institutions like government or research institutions. 
 In this dashboard we will look at various aspects of study activities of sponsors.
Figure 5.1

1. How many sponsors have registered clinical trials in the US? How many of them are from the Industry (Commercial)? How many studies have they registered? For how many studies did the sponsors from commercial sector have posted the results for the studies?
The tiles on the top provides few sponsors related summary metrics to answer some of the questions mentioned above.
There are a total of 313,345 studies registered by 28,068 lead or primary sponsors in the US till date. Out of 28,068 sponsors, 8,717 sponsors are from commercial sector with 81,169 studies registered and the remaining 19,351 sponsors are from non-commercial sector with 232,176 studies registered. 
There are 4,545 sponsors with at least one study result posted and 1,680 of them are from Industry. 

2. What percentage of studies were registered by sponsors from industry as compared to the non-industry? 
About 26% of studies were sponsored from the industry or commercial sector. A small percentage 3.31% and 1.16% are contributed by NIH (National Institute of Health) and US government respectively. The raw data did not provide further classification into the non-industry sector. The data is transformed to figure out if the non-industry sponsor is a Hospital or University/Institute/School. The shows that Universities have been a major source of sponsored studies with almost 45% share and Hospitals having 9% share.

3. What's the growth in number of studies sponsored by study as compared to the non-industry sector over the last few years?
Except 2008 and 2014, the number of studies registered by Industry sponsors have largely remained stable around 5,500 mark. In contrast, the studies registered by non-industry sponsors have grown rapidly. Notice the size of the steps in the chart. Also notice the increasing gap between the two lines.

4. What percentage of registered studies have some participation from industry?
The pie chart named Industry Participation shows the share of studies where either the primary sponsor is from industry or at least one of of the collaborators is from industry. About 33% of the studies has some participation from industry.
 
5. Who are the top performing industry sponsors?
The tabular chart shows the primary sponsors from industry sector ranked based on the number of studies registered. The chart also display metrics like number of countries they have recruited patients, number of recruiting facilities, studies in completed state, studies where the recruitment has not yet started, studies that are currently recruiting and studies where results are posted. The success ratio compares the studies that were registered minus the studies that have not yet started or are in progress with the completed studies.
GlaxoSmithKline(GSK) is the top performer with 3351 studies and 91% success ratio followed by Pfizer and Novartis. Pfizer has recruited patients in 105 countries. Sanofi is another sponsor that recruited patients in 107 countries. 

6. Who are the top performing sponsors from non-commercial sector?
National Institute of Health Clinical Center, National Cancer Institute and M.D Anderson Cancer Institute are top 3 performers. The non-industry sponsors have recruited patients in fewer countries as compared to the top sponsors from commercial sectors.
The dashboards can answer many other questions by simply slicing and dicing the data by different dimensions.
If you get any questions in your mind that you want to share, please post them in comments and I will try to address them.
Till next time.  

Wednesday, August 28, 2019

Clinical Intelligence Analytics - Study Trends

Study Trends

Study Trends dashboard (Figure 4.1) gives us insights into the tends in recruiting country, average registration to enrollment duration and average study duration over the past 2 decades.
Figure 4.1

The data legends are shared between the charts on the first row. Similarly, the legend is same for the 2 charts on the bottom row.
The data is aggregated on a study level and a study is classified as an International (Both US and non-US), US-only and non-US only study based on the countries of patient recruitment. The analysis excludes studies that does not have any recruiting country information which could be for various reasons such as the recruitment might not have started or the study may not have any enrollments yet.
An international study means that it has recruited patients in the US and at least one other country. 
A non-US only study means that the study has recruited the patients in countries other than the US and no patient was enrolled in the US.
For the other 2 charts on the bottom row, the numbers with a minus sign are positive numbers but are shown as negative numbers just for the display purpose as they are on the opposite side. However, this is not intended. The vertical lines are the average lines to show the distance.

The dashboard can provide insights into the following trends:
1. What's the share of studies by recruiting country?
55% of the studies registered in the US have recruited the patients only from countries other than the US. The share of studies that recruited the patients only inside the US is 39%. International studies are just 6%.


2. What is the trend in the study registration by their location of recruitment?
Now that we know something about the share of the studies based on where the patients were recruited, let's take a look at how it has changed over the last 2 decades. The share of international studies has reduced to less than 5% now from 15% in early 2000's. The trend of US-only studies have also declined sharply from lower 90% in early 2000's to 30-35% level now. The trend of non-US studies have increased consistently in past 2 decades from 44% in year 2005 to 66% in 2019.  
Remember that the share of the studies registered in the past years can change based on the studies that are still recruiting or may recruit in future. Hence, the current trend is the snapshot.

3. How has the average time taken study registration to enrollment changed over the last few years?
The chart shows the trend in the time taken from study registration to patient enrollment or study initiation. The chart also compares side-by-side the duration for studies sponsored by industry or non-industry sponsors.
There are many studies that were registered retrospectively, meaning the studies were registered after they were already started (the first patient was already enrolled). Such retrospective studies were excluded from the analysis. Only for the prospective studies, the registration to enrollment duration is calculated in days.  
It appears that it usually took longer, sometimes 1.5-3 times, for non-industry sponsored studies to begin a study after they are submitted. The trend for non-industry sponsored studies is following a parabolic curve. The average registration to enrollment duration for the non-industry sponsored studies is 125 days which is higher than the overall industry average of 107 days. For the most part, the yearly trend is close to the average line except in year 2010 having an average of 145 days, which is also the highest in recent years.
On the other hand, the industry sponsored studies are initiated quickly and the study initiation duration has improved slightly overall. The average for industry sponsored studies is around 80 days which is well below the industry average of 107 days. The average for the last few years has been consistently near the average line.   

4. How has the average study duration changed over the last few years?
The non-industry sponsored studies takes longer to complete as compared to industry sponsored studies. The average study completion duration for non-industry sponsors is close to 3.5 years which is considerably much higher than the overall industry average of 2.6 years. On the other side, the average for industry sponsors is little above 2 years. The good news is that both type of sponsors have made a significant improvement is past 15 years to bring down the average completion duration to lower levels, possibly signalling great improvements in overall operational efficiency in study conduct.
With that positive note, see you till next time. 

Friday, August 23, 2019

Clinical Intelligence Analytics - Study

Study Dashboard


In study dashboard (Figure 3.1), we will look at certain aspects of study at aggregated level as well as at a study level. 
Figure 3.1

The study dashboard will try to answer following questions:

1. What is the average study completion duration for sponsors from Industry and non-Industry?

For all types of studies (All), the sponsors from Industry completed the studies in about 1.9 years. In comparison to that, sponsors from non-industry took almost 3 years to complete the study.
The observational studies (Obs) took longer to complete. The Industry sponsors with an average of 2.3 years performed fairly better than the non-industry sponsors with an average of 3.2 years.
For interventional type of studies (Int), the average study took 1.8 years for Industry sponsor as compared to 2.9 years for non-industry sponsors.
We may further want to look at the study duration by the phase of the study. Phase 3 studies are large scale and complex in nature and hence, it should take longer to complete when compared with phase 1 and phase 2 studies. Let's see what we find. Only interventional studies go through the drug development phases. If you take a look at Avg Study Duration by Phase chart, Phase 2 studies took longest among all the study phases with an average of 3.3 years. Phase 3 studies took an average of 2.9 years to complete where as phase 4 studies took 2.4 years. Early phase 1 studies took longer than the phase 1 studies.

2. What is the share of sponsors from industry and non-industry in interventional or observational studies?
Almost 80% of studies were interventional studies. 56% of 80% which 70% of total interventional studies were sponsored by non-industry sponsors. The industry sponsors have greater share in interventional studies as compared to its share in observational studies.

3. What percentage of studies were completed between 0 to 3 years or between 8 to 10 years?
40% of the studies were completed between 1 to 3 years. Around 29% studies were completed in less than 1 year. 

4. Which studies took the longest to complete?
There are 44 studies (0.02%) that took more than 30 years to complete. The study that took longest was sponsored by Johnson & Johnson to evaluate the efficacy of oral Levofloxacin in the treatment of chronic Bronchitis. This study took 63 years to complete starting in 1931 and completing in 1994 and has enrolled 367 patients. 

5. At study level, how many medical conditions a particular study is conducted?
See the tabular report to view the number of enrollment, medical conditions and the number of study sites and countries of subject recruitment.

6. In how many countries and facilities did a study recruited patients?
See the tabular report.
The dashboard will show the description of the selected study.

Sunday, August 11, 2019

Clinical Intelligence Analytics - Trends by Study Attributes

In the last post, we looked at the growth trends of studies registered, initiated, completed and posted results over the period of last 20 years. We looked at yearly trends and then drilled down at quarterly and monthly trends and compared the growth in current year with the previous year.
In this post, we will see the growth trends of registered studies by study attributes like study type, study phase, Drug/Device and DMC flag over the period. I have filtered out the studies where the study attributes were not specified.
Figure 2.4

This dashboard (Figure 2.4) is an extension of growth trends:
1. Study Submission Trend by Study Type-
The chart shows the trend of studies submitted for interventional and observational types.
The share of interventional studies have decreased. In early 2000's, there were around 90-93% interventional studies and 7-10% observational studies. In last few years, the share of observational studies have increased to 21%.

2.  Study Submission Trend by FDA oversight-
The chart shows the trend of studies by the oversight of the FDA, if the study is for FDA regulated drug or a device. 
Until 2008, the share of the studies for FDA regulated devices was less than 10% which has increased to around 25% now.

3. Study Submission Trend by Study Phase-
 Phase 3 studies are important studies since sponsors apply for FDA approval after that. 
Study type NA are the studies that do not have a phase of a study, and I guess it is mainly for the device related studies. These studies share have increased significantly over the period and I think its because the device related studies share have increased as we observed in the previous chart.
There is a slight drop in the share of phase 1 studies. The share of Phase 2 studies in green has decreased from 43% in 2003 to 12% in 2018. Phase 3 studies have also followed the same trend with the share reducing to just 7% in 2018 from 25% in 2005. Phase 4 are post marketing studies and the share has reduced from 16% in 2005 to 7% in 2018.

4. Study Submission Trend by DMC-
The DMC flag tells if the study has a Data Monitoring Committee appointed or not. There were many studies that did not mention if they have DMC or not. As I mentioned in the beginning, the chart is the representation of only studies that has the data and others were filtered out.
The share of DMC appointed studies increased in the first few years and then start to drop until 2008 after which it picked up again a bit and maintaining the 40% level until 2013 but falling down a bit to 34% in 2018.
Feel free to share your thoughts.
See you soon in the next post.
  

Saturday, August 10, 2019

Clinical Intelligence Analytics - Growth Trends

Trial Growth Trends Dashboard


Growth Trends Dashboard provides insights into the growth trends of clinical trials over a period of time. This helps us gauge how the industry is growing. 
Below (Figure 2.1) is a snapshot of the dashboard without any data filters. Figure 2.2 is another representation to view the Year over Year growth. Year 2019 is the current year and hence the decline should not be viewed as negative growth. We still have few months remaining in 2019.
Figure 2.1

Figure 2.2

The Dashboard has the same summary tiles on top of the dashboard except a new metric to measure average number of days from registration to study initiation or enrollment. The average for prospectively registered studies is 107 days, which means that it takes 107 days on an average for a study to enroll its first patient after it has been registered.

Broadly, there are 4 times that are important milestones from study registration to the posting of results. The trends in this dashboard shows these 4 important milestones. The Growth Trends Dashboard can answer some of the following questions:
1. How the study registration in the US has grown over the last 20 years?
Registering the study is the first step and hence, it helps us in understanding how the industry is growing. A decline in study registration would mean less successful drugs or devices reaching the market. With patented drugs losing patent protection, a declining product pipeline can negatively impact the growth of the industry. CRO(Clinical Research Organisations) conduct the clinical trials on behalf of the sponsors and hence a decline in study registration can put brakes on the growth of CRO industry.
The study registration trend is increasing consistently except in year 2005 and 2008 that saw a sudden jump. International Committee of Medical journal Editors(ICMJE) began requiring trial registration as a condition of publication in September 2005. This explains the jump in 2005. The jump in year 2008 could be related to the recession period.
Beyond 2008, there has been consistent growth sometimes in double digits. The outlook for the industry as a whole looks positive.

2. Has the growth in the studies initiated been consistent?
Sponsors take lot's of efforts in initiating a study. It's a commitment they make in terms of money and efforts and hence it is an important indicator to see the growth in study initiation. The average duration for a study to go from registration to initiation is 326 days.
The growth in number of studies initiated over the last 20 years is also consistent until 2016. The growth has declined in last 2 years around -6.5% YOY. Year 2019 may also end up following the declining trend. The rate of YOY growth has consistently gone down from 42% in 2002 to -6.5% in 2018. If the trend continues, the coming years may prove to be difficult for the industry and companies need to start looking at alternatives to increase the product pipeline.
3. Are studies being completed growing consistently?
Completing the study is like clearing a big hurdle in drug development. Conducting a study is lengthy, costly, complex and risky and hence a successful completion is a big milestone and a big relief to sponsors.
The growth in studies completed over the last 20 years has been positive and consistent until last year 2018 when the growth was negative. The rate of growth declined consistently after 2007 with a recovery in 2014. The rate of growth came down to 1% in 2017 and then dropped to -8.5% in 2018. The current year 2019 doesn't look to be making any recovery. With just few months remaining, 2019 is 64% away from last year 2018. 
4. Are sponsors submitting study results growing?
ClinicalTrials.gov launched the results database in September 2008 and hence sponsors started posting the results after that. 
The trend shows that the posted results increased at a very high rate until 2014 recovering 39% in 2017 but again declined 20% in 2018. Current year 2019 seems to be matching up but it is yet to be seen if it will end with a positive growth.
If you notice, I compared the current year 2019 with last year 2018 to get an understanding of the current year performance. I did get some fair idea but I wanted to go one level down and see the current year has performed on a quarterly and monthly basis as compared to the last year. I wanted to see if there is any trend where there is high activity in certain months, so I created a dashboard which can provide some insights into understanding the current year performance in Figure 2.3.
Figure 2.3

The four tabular reports on the top row compares the monthly comparisons of current year months with previous year months. The increase column is the difference and appear in green or red based on whether the change is positive or negative. The bar charts on the bottom row compares the same metrics on quarter basis. Remember, August is the current month and hence the third quarter will not have complete values.
Let's take a look at all 4 metrics one by one and make some observations.
1. Study Submissions:
Current year has performed well so far and the number of studies have maintained a positive growth when compared with the same period of last year. Observe that last August had the highest number of studies submitted and unless there is a trend to submit the studies in the last few days of the month, we can expect August to play fairly well but may not be able to exceed. The lead current year has maintained in the first 2 quarters may help to gain a positive growth this year in number of studies submitted.
2. Studies Initiated:
So far, not a single month with a positive growth and the current year months have unperformed with a large margin. There are no months in the remaining period with unusually high or low activity and so if the trend continued, we may see a large drop in the 2019 study initiations as compared to 2018. I will keep an eye on that in the coming months and share with the readers here.
3. Studies Completed:
The monthly and quarterly numbers looks disappointing similar to study initiation. December month has high numbers possibly due to year end activities so we can expect some improvement in filling in the gap but the overall outlook doesn't look promising. 2019 may end up with a significant drop as compared to 2018.
4. Study postings:
The first two quarters have performed well and the current quarter also looking good. Hopefully, 2019 would see some positive growth. 
With that positive note, see you till next time. 


Friday, August 9, 2019

Clinical Intelligence Analytics - Summary

Clinical Summary Dashboard


Summary Dashboard gives an overall picture of clinical trials in a summarized form at a high level. 
Below (Figure 1.1) is a picture of the dashboard without any data filters. If I make any selection or filter, I will call it out and mention it.
Figure 1.1


The Dashboard tries to answer some basic questions to start with, and then we start looking at things from different angles and dimensions. 
The summary Dashboard can answer some of the following questions:

1. How many studies have been registered so far in the US?
This the total number of studies registered in the database. As on 09-Aug-2019, there are 313,345 studies registered in the US.

2. How many studies did actually started?
A study is considered to be started when it enrolls its first patient. It's an important milestone in the entire clinical trial process. 291,364 out of 313,345 which is around 93% of the studies did actually start by enrolling a patient.

3. How many studies did actually completed? 
Another important milestone is when a study completes and the patients who participated in the study stops receiving the drug. Of the 291,364 studies that started, 167,511 studies were completed, which is 58%. 

4. For how many studies did the sponsors posted the results?
Once the study is completed, the data collected is analyzed and the results are posted. Results Database was initiated in 2008 whereas the study registration began in 2000, so there might be studies without posted results. 38,127 studies have results posted out of 167,511 completed studies which is 23%.    

5. How many studies are currently recruiting patients?
A study recruits patients as study facility location called study sites. These study locations could be in many countries. 54,968 studies are presently enrolling patients including the ones that are enrolling only by invitation. This means 19% studies of the 291,365 studies that were started are still recruiting patients. 

6. How many patients were recruited in the past?
There were few enrollment values such as 99999999 that were converted to 0. About 490 Million people participated in the clinical trials across the globe from 210 countries. As per the recent United Nations estimate, the would population is 7.7 billion. We can say that 6.4% of world population has participated in clinical trials of the US. Other countries may have their own clinical trials registry.

7. What is the average duration of study completion?
Duration is the difference in the start and completion date of the study. 2.62 years is the average duration for a study to complete. Phase 3 trials are large scale studies and takes longer than phase 1 and 2, but we will look at that later. We can say that it will take around 8 years for a new drug to complete all the phases of clinical trials before it can apply to FDA for approval. Add another year or 2 for pre-clinical testing of the drug on laboratory animals. Now I understand how lengthy, complex and risky is the entire process of drug development. I will not go into the drug pricing strategies but you got a sense why those drugs are so un-affordable, even with insurance sometimes.

8. How many total sponsors registered the studies?
28,068 sponsors from both industry and non-industry (government agencies etc) have registered studies. We will see the ratio and proportions later.

9. What share of registered studies were interventional or observational?
Almost 80% of the studies are interventional studies where some kind of therapy is given to the participant.

10. What percentage of registered studies were sponsored by industry and non-industry sponsor?
Non-Industry sponsors leads with 3/4th of studies sponsored by them.

11. Top 10 sponsors who registered the most studies?
GSK is the leader. Pfizer and Astrazeneca are other sponsors from pharmaceutical industry following with a close margin. National Cancer Institute, a non-industry sponsor, is at a second position. 

12. What are the top medical conditions for which the studies were registered?
Surprised to see obesity at number 2. Asthma and depression are in top 10. I never thought they were so important but I guess our lifestyle changes are responsible for their growth. Breast cancer is the most studied medical condition.

13. What is percentage share by the overall status of the study?
Only a small portion of the studies were withdrawn and suspended, however, 5.65% studies were terminated which could be a cause of concern.

14. What are the top 10 countries that recruited the patients?
US has recruited about 18% of the total participants. 
Taiwan at no 2 surprised me. I found it enrolled around 67 million participants for an observational study but Taiwan's total population is around 25 million. The enrollment number is an outlier to me, however, I did not change it. Cambodia too has a study that enrolled 15 million participants for an observational patient registry sponsored by non-industry sponsor French National Institute. 
Since observational studies enroll large population of participants, let's look at who are the top countries who recruited for interventional studies only (Figure 1.2). Almost 82 million participants have been enrolled so far and US once again leads the chart with a contribution of little over 13% and China closing the gap at second position.   
Figure 1.2


You can always slice and dice the analysis to look at things from different perspective in a dashboard. It's real fun to create your own questions in your mind and then try to find out the answers yourself.

See you till next time.

Clinical Intelligence Analytics - Insights

Clinical Trial studies a new drug or device before it is brought to the market. The new therapy is tested on human subjects to evaluate its safety and efficacy.
Sponsors or investigators of certain clinical trials are required by U.S. law to register their trials on and submit summary results to ClinicalTrials.gov website. 
While working for a CRO as a Business Intelligence and Data warehouse Engineer, I gained some basic knowledge about the Clinical Research. I got so much interested that I decided to study Bio-sciences Management and Analytics subjects in my graduate MBA program. Unfortunately, my curiosity and the desire to learn more about Bio-sciences did not end there. 
I am passionate about creating insights out of data and I always try to unravel the layers of my curiosity by diving deep into the data. So, I decided to get the data from ClinicalTrials.gov and create Clinical Intelligence Analytics for myself. Here is the link in case you want to download it too.: https://aact.ctti-clinicaltrials.org/
The objective of creating this application is to share the insights with the community so that they know more about the things happening in this space. I would be really happy if this application could be of any benefit to patients, physicians,sponsors and other partners of the ecosystem. There are few online websites that helps patients find the recruiting study. However, I did not find any easy way that can help patients find out more about particular studies or sponsors or investigators in the past so that they can make informed decisions.
I used Talend software to get the data and used Qlikview BI to do data preparation and to create analytic dashboards. I have created more than a dozen dashboards so far and creating more as we go along. 
I would appreciate to leave a comment if you read the posts and find it useful. 
Since I do not want to make the posts boring for readers by putting a lot of information in one single post, I would be posting multiple posts in a series in coming days and update the link below in this post.

1. Clinical Summary Dashboard
2. Growth Trends Dashboard

Here are few links that would help in understanding basic terminology and basic information on ClinicalTrials.gov:
Common Terms
Trends Charts

Friday, April 6, 2018

Blockchain for Healthcare and Clinical Trials

Blockchain for Healthcare and Clinical Trials by Manohar Rana



The article is based on our 3rd place winner's proof of concept presented at Generation Blockchain Challenge.

          In general, healthcare and clinical trials are complex business environments mainly due to its direct impact on the human lives and various regulations built around them. There are various stakeholders in the entire ecosystem, and the need to improve on how these stakeholders collaborate and communicate with each other is ever increasing. Technological advancements from time to time have made significant improvements, but due to slow adoption of these technological advancements in healthcare in general, there is a great potential for newer technologies like blockchain to bring significant improvements in the overall systems.
          Healthcare organizations have made significant improvements through technological and process innovations that have benefitted and improved the entire customer experience. The most important customer in the ecosystem is a patient, and the entire healthcare business is centered around this customer. The ultimate aim of the various players like physicians, clinics/hospitals, pharmacies, drug manufacturers (pharmaceutical companies) is to bring value to a patient and enhance the overall customer experience. Then there are regulatory bodies like Food and Drug Administration (FDA), that oversees all these players, ensure the rights of a patient are protected and that they not misused in any way. A patient is the end consumer of the benefits in the entire value chain.
          On the other hand, in clinical trials, the drug manufacturer companies actually partners with human subjects aka patients to try their trial drugs on them before they bring the new drug to the market. Some of the key players in the clinical trials process are the Pharmaceutical company or the drug manufacturer, Contract Research Organisation (CRO) and Site Investigators (Physicians). Institutional Review Board (IRB) act as a regulatory body under the FDA. Since the other actors in the ecosystem are organizations that have their own technological infrastructure, the subjects remain at the receiving end. They have a limited role to play in the entire process and is limited by the technological capabilities of other's systems. Regulatory requirements make Organizations business systems slow, complex and inflexible. Generally, both healthcare and clinical trials partners have greater needs to collaborate and share the information through these complex systems.
          Attempts are made from time to time to come up with centralized systems that can facilitate greater collaboration and quick information sharing, but such systems pose their own challenges of ownership of data. Integrating data from different systems owned by different parties is a challenge. One alternative way could be to try to connect the trusted parties that are known to each other on a common platform. Blockchain technology has the potential to play that role. It may be too early to predict what role blockchain can play since there are not enough use cases that are being tried upon. It is difficult to say if Blockchain can displace the existing systems completely or complement them for some time before it actually does that. The objective here is not to speculate that possibility of whether Blockchain is a replacement for traditional Clinical Trial Management Systems but to explore the possibilities of small use cases that can actually bring value to the entire ecosystem.
     
Before we discuss how Blockchain can play an important role in clinical trials, it is important to understand the current challenges in the healthcare and clinical trials.

Few of the challenges in clinical trials are:

1. Subject Recruitment: To ask and convince a healthy subject to try a new trial drug is a challenge. There could be different motives for a healthy person to take that risk for monetary or personal reasons. Sponsor's find it very difficult to identify and recruit ideal subjects. A lot of times, the self-reported information provided by subjects cannot be authenticated leading to issues like dual enrollment, false disclosures, higher screen failures, a potential risk of severe adverse events (SAE's), and lawsuits leading to increased cost and bad quality of clinical research trial data.

2. Conducting trials: Sponsors make changes to the study protocols modifying inclusion and exclusion criteria mentioned in the study protocol after the study has started. At certain times the changes are genuine but sometimes the changes are made to widen the inclusion criteria or narrow down the exclusion criteria so that more subjects can be recruited easily.

3. Lack of trust and transparency.

4. Challenges in collaboration and communications.

Blockchain will increase and establish the trust in clinical research by the fact that tempering and manipulating the research data in blockchain is very difficult and easily traced. Self-reported data by the subjects generally lacks trust, which ultimately impacts the quality and cost of the drug trial. There is lack of trust in the way clinical research data is gathered, analyzed, and reported. Trust is further decreased because of unethical and unprofessional practices such as altering and not reporting the inclusion and exclusion criteria in a protocol to suit the interests of drug manufacturers. The timestamped block transactions can be easily traced and verified, making it less prone to manipulation and tempering. It would be worth reading the article about blockchain timestamped protocols here.
Blockchain will increase the transparency, collaboration, and communication in clinical trials. There are many partners in the clinical research ecosystem like Pharmaceutical companies(sponsors), CRO’s, study investigators (Physicians), hospitals, laboratories, insurance providers and patients, and there is a great need for all partners to collaborate and communicate effectively because human health is at stake.  The challenge is that every partner has their own technology systems which limit their ability to communicate effectively and efficiently. A lot of time and money is wasted in requesting, transferring, and communicating the information between different systems.
Blockchain brings all the trusted parties in the ecosystem to a common platform enabling them to see the clinical health records flowing through the system in real time and make timely decisions.
Not only that, Once the identity of a subject is established in the blockchain network, blockchain also addresses the issues related to subject’s dual enrollment in multiple studies at the same time saving the subject from being misused and exploitation. It is very difficult to find if a subject has enrolled in other studies. Ed Miseta, in his article, has highlighted the issue of dual enrollment in great detail here.
From sponsor’s perspective, it saves them lot of efforts wasted in subject recruitment causing higher screen failures.
Another important aspect of blockchain is that it enables a patient to play an important role as a participant. Currently, a subject is always at the receiving end of the value chain and has very limited or no access to his information. For example, in case of an adverse event, once a patient’s adverse event is notified to the physician, the patient has no idea how his case is followed up by a physician with other stakeholders. Blockchain system facilitates a patient to become an important participant in the whole ecosystem.

The inherent architecture and advantages of blockchain will make various processes and systems irrelevant and unnecessary, making the overall process of clinical research simple and cost-effective. The direct impact of this will be that it will help in bringing down the overall cost of bringing a new drug to the market, which ultimately will be passed on to the patients. More importantly, a subject would become a key participant in the clinical trial process and would be saved from misuse and exploitation.

Blockchain technology has the potential to bring disruptive changes in healthcare and clinical trials, that would make many of the current processes and businesses obsolete. It's in the best interest of the entire industry to explore the opportunities blockchain provides to remain sustainable in the longer run.