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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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 Clinical Trial for Patients with Advanced Cancers
Corbus Pharmaceuticals Holdings
Advanced Solid tumour
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 1/2a, First in Human, Open-Label, Multicenter, Dose Escalation Study with Expansion Cohorts to Evaluate the Safety, Tolerability, and Preliminary Activity of LB101 in Subjects with Advanced Solid Tumors
Centessa Pharmaceuticals plc
Advanced solid tumors
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 I, open-label, multi-center exploratory safety and efficacy study with PSMA, SSTR2 and GRPR targeted radioligand therapy in metastatic neuroendocrine prostate cancer
Novartis Pharmaceuticals
Metastatic neuroendocrine prostate cancer
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 -
A sterile preservative-free solution with identical composition as the drug product, but without the protein.
Kiniksa Pharmaceuticals International, plc
Sjögren’s Disease
1 trial -
A-623
Santhera Pharmaceuticals (Deutschland) GmbH
Systemic Lupus Erythematosus
1 trial -
A006
Amphastar France Pharmaceuticals
Asthma
1 trial -
A006 DPI
Amphastar France Pharmaceuticals
Asthma
2 trials -
ABIRATERONE, DAROLUTAMIDE, DZR123, -, -, ABIRATERONE, DZR123, DAROLUTAMIDE
Novartis Pharmaceuticals
Metastatic hormone-sensitive prostate cancer
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 -
ACE-536
Celgene Europe Limited
Beta-Thalassemia
1 trial -
ACE393
Fulcrum Therapeutics
Campylobacter Infection
1 trial -
ACETYLCYSTEINE , DEXAMETHASONE , DIPHENHYDRAMINE , GLUCOSE
Inhibrx Biosciences
Unresectable or metastatic conventional chondrosarcoma
1 trial -
ACP-044 Dose A
Acadia Pharmaceuticals B.V.
Acute Postoperative Pain
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