Intelligence · Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors — phase, modality, and trial IDs for BD and competitive intelligence.
- Programs indexed
- 20,548
- Companies
- 1,769
- Drugs tracked
- 4,797
Quick answer
NovaPharmaNews tracks 20,548 pharmaceutical R&D pipeline programs sourced from ClinicalTrials.gov, linked to sponsor companies. Each profile includes development phase, modality, trial status, NCT identifiers, and indication text — searchable for business development and competitive intelligence.
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risankizumab placebo, Risankizumab, ABBV-066 / Risankizumab, ABBV-066
AbbVie Deutschland GmbH & Co. KG
Ulcerative Colitis
1 trial -
tulisokibart, Placebo to Subcutaneous or intravenous MK-7240 (Tulisokibart), tulisokibart
Merck Sharp and Dohme
Crohn’s Disease
1 trial -
tulisokibart, tulisokibart, Placebo to MK-7240
Merck Sharp and Dohme
Ulcerative colitis
1 trial -
ublituximab, DEXAMETHASONE, PARACETAMOL, GADOBUTROL, ublituximab placebo, DIPHENHYDRAMINE, CETIRIZINE, METHYLPREDNISOLONE
TG THERAPEUTICS, INC.
Relapsing multiple sclerosis
1 trial -
xevinapant, Xevinapant Placebo
Merck Sharp and Dohme
Resected squamous cell carcinoma of the head and neck
1 trial -
ziltivekimab, Placebo (ziltivekimab C)
NovoThirteen
Heart failure with mildly reduced or preserved ejection fraction and systemic inflammation
1 trial -
Placebo to Osimertinib - Film-coated tablet - 40mg / 80mg, CARBOPLATIN, TAGRISSO 80 mg film-coated tablets, CISPLATIN, PEMETREXED, PEMETREXED, TAGRISSO 40 mg film-coated tablets
AstraZeneca AB
Non-Small Cell Lung Cancer
1 trial -
(+)-α-DIHYDROTETRABENAZINE, ADE513 placebo
Lacuna Pharma Pty Ltd
Tardive dyskinesia
1 trial -
-, DNL593 Placebo, Sterile lyophilisate in single-dose glass vials, -, FAMOTIDINE
Denali Therapeutics
Frontotemporal Dementia (FTD)
1 trial -
10 mg PRAX-114, 20 mg PRAX-114, and Placebo
Chongqing Precision Biotech Co., Ltd
Essential Tremor
1 trial -
6QC-ICG, Placebo for 6QC-ICG
Disc Medicine
Breast cancer
1 trial -
A 52-week randomized, double-blind, placebo-controlled, multi-center Phase 2b study with a 52-week blinded extension and an optional open-label extension—assessing the safety and efficacy of frexalimab, a CD40L-antagonist monoclonal antibody, for the preservation of pancreatic β-cell function in adults and adolescents with newly diagnosed type 1 diabetes on insulin therapy
Sanofi-aventis Healthcare Pty Ltd
Type 1 diabetes mellitus
1 trial -
A Dose-Finding, Adaptive, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-360 in Participants with Idiopathic Hypersomnia (IH)
Takeda
Idiopathic Hypersomnia (IH)
1 trial -
A Dose-Finding, Double-Blind, Placebo-Controlled Phase 2 Study to Evaluate the Efficacy and Safety of GSK4532990 for Steatohepatitis in Adults with Alcohol-related Liver Disease (ALD)
GlaxoSmithKline
Liver Diseases, Alcoholic
1 trial -
A Phase 2, Dose-finding, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of Efavaleukin Alfa Induction Therapy in Subjects with Moderately to Severely Active Ulcerative Colitis
Amgen
Ulcerative Colitis (UC)
1 trial -
A Phase II, 6-week, multi-centre, randomised, double-blind (participant and investigator), placebo-controlled, dose-finding trial to evaluate the efficacy, tolerability, and safety of different doses of oral BI 1569912 as adjunctive therapy in patients with major depressive disorder
Boehringer Ingelheim
Major depressive disorder
1 trial -
A Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy of Fenebrutinib in Relapsing Multiple Sclerosis
Hoffmann-La Roche
Relapsing Multiple Sclerosis
1 trial -
A Randomized, Double-Blinded, Placebo-Controlled, Dose-Finding, Adaptive Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-360 in Participants with Narcolepsy without Cataplexy (NT2)
Takeda
Narcolepsy without Cataplexy (NT2)
1 trial -
A double-blind, randomized, placebo-controlled, dose-finding phase II study to assess the efficacy and safety of pasireotide s.c. in patients with Post-Bariatric Hypoglycaemia
Recordati Ireland
Post-Bariatric Hypoglycaemia
1 trial -
A parallel-group treatment, Phase 2a, multicenter, randomized, double-blind, placebo-controlled umbrella study to evaluate the efficacy and safety of frexalimab, brivekimig and rilzabrutinib in participants aged 16 to 75 years with primary focal segmental glomerulosclerosis (FSGS) or minimal change disease (MCD)
Sanofi-aventis Healthcare Pty Ltd
Immune system diseases
1 trial -
A phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the safety, tolerability, and efficacy of S-337395 in symptomatic nonhospitalized adults with respiratory syncytial virus who are at high risk of progression to severe disease
Shionogi B.V.
Respiratory Syncytial Virus
1 trial -
A randomized, double-blind, placebo-controlled, dose-ranging Phase 2 study of brivekimig followed by a maintenance period in participants with moderate to severe hidradenitis suppurativa
Sanofi-aventis Healthcare Pty Ltd
Hidradenitis suppurativa
1 trial -
AC102-Suspension 12 mg/ml, placebo gel, Placebo matching Prednisolone, Prednisolon 10 mg GALEN®
Lacuna Pharma Pty Ltd
Idiopathic Sudden Sensorineural Hearing Loss
1 trial -
ACT-1004-1239 matching placebo
Lacuna Pharma Pty Ltd
Progressive multiple sclerosis (MS)
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 20,548 clinical development programs grouped by sponsor company, with phase (Phase 1–3), modality, trial status, and linked NCT IDs from ClinicalTrials.gov.
Where does pipeline data come from?
Program records are derived from ClinicalTrials.gov and linked to NovaPharmaNews company profiles. Trial status and phase reflect registry data at last sync — verify on ClinicalTrials.gov before investment or partnering decisions. See our data sources page for attribution.
How do I find pipeline programs by company or phase?
Use the search box to match program name, indication, company name, or slug. Results are ordered with late-stage (Phase 3) programs first. Open any row to view the full program profile under its sponsor company.
Data attribution and licensing: Data sources