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- United Therapeutics Europe · 219 programs · 43 late-stage
Intelligence · Clinical Development
Clinical Development Intelligence
Pipeline intelligence, regulatory progress, and competitive landscape — not a flat database. Track phase distribution, catalysts, and sponsor rankings across indexed programs.
Quick answer
NovaPharmaNews Clinical Development Intelligence tracks 20,548 pharmaceutical pipeline programs from ClinicalTrials.gov with phase distribution, therapeutic area hubs, NDA/BLA watchlists, upcoming readouts, company rankings, and competitive landscape views — designed for BD, investor, and regulatory teams benchmarking against Evaluate Pharma, Citeline, and GlobalData.
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Latest indexed programs
Recent programs from the index — each links to a sponsor program profile with hub cross-links. Browse Phase III hub
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NN9490-8021
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Obesity
1 trial -
NN9490-8024
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Overweight or obesity, and type 2 diabetes
1 trial -
NN9490-8025
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Overweight or obesity, and obstructive sleep apnoea not treated with positive airway pressure
1 trial -
NN9490-8026
NovoThirteen
Overweight or obesity, and knee osteoarthritis
1 trial -
NN9490-8028
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Participants with overweight or obesity, and type 2 diabetes
1 trial -
NN9490-8266
NovoThirteen
HFpEF or HFmrEF and obesity
1 trial -
NN9490-8293
NovoThirteen
Overweight or obesity, and obstructive sleep apnoea treated with positive airway preassure (PAP)
1 trial -
NN9490-8294
NovoThirteen
Overweight or obesity, and knee osteoarthritis
1 trial -
NN9490-8559
NovoThirteen
Obesity
1 trial -
NN9535-4352
NovoThirteen
While it is well-established that long-term good glycaemic control will reduce the risk of diabetic retinopathy development and progression, intensification of glycaemic control has also been associated with an initial worsening of diabetic retinopathy. This phenomenon is known as “early worsening”. The rationale of this trial is to establish the long-term effects of semaglutide on diabetic retinopathy in subjects with type 2 diabetes (T2D) using validated and standardised ophthalmic assessments. This trial is a post-authorisation safety study (PASS) conducted as a commitment to the European Medicines Agency
1 trial -
NN9535-4801
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Participants with T2D and overweight
1 trial -
NN9833-8242
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Overweight and obesity
1 trial
Frequently asked questions
What is the Clinical Development Intelligence Platform?
It is NovaPharmaNews pipeline intelligence hub covering 20,548 clinical development programs — not just a directory. It includes phase distribution dashboards, therapeutic area overviews, NDA/BLA watchlists, upcoming readouts, company pipeline rankings, competitive landscape maps, and personalized watchlists.
How does this compare to Evaluate Pharma or Citeline?
Like Evaluate Pharma and Citeline Trialtrove, we index ClinicalTrials.gov programs by sponsor, phase, and indication. Our platform adds cross-links to NovaPharmaNews company profiles, drug INN pages, patents, and congress readout calendars — improving crawl depth and reducing orphan program pages.
Where does pipeline data come from?
Program records derive from ClinicalTrials.gov and link to sponsor company profiles. Trial status and phase reflect registry data at last sync — verify on ClinicalTrials.gov before investment decisions. See our data sources page for attribution.
Can I follow a company or program for updates?
Yes — use the watchlist forms on this page to follow sponsors, individual programs, disease clusters, or therapeutic areas. Alerts use the same subscription infrastructure as our events intelligence hub.