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
- 18,156
- Companies
- 1,062
- Drugs tracked
- 3,385
Quick answer
NovaPharmaNews tracks 18,156 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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XEOMIN 200 jednotek prášek pro injekční roztok, XEOMIN, 200 jednostek, proszek do sporządzania roztworu do wstrzykiwań, XEOMEEN 200 eenheden poeder voor oplossing voor injectie, XEOMIN 200 egység por oldatos injekcióhoz, XEOMIN 200 jednotiek prášok na injekčný roztok, XEOMIN 200 unidades polvo para solución inyectable, XEOMEEN 200 unités poudre pour solution injectable, XEOMIN 200 Einheiten Pulver zur Herstellung einer Injektionslösung, XEOMIN 200 unités, poudre pour solution injectable, XEOMIN, 200 unità,
Merz Pharmaceuticals GmbH
Lower limb spasticity
1 trial -
ZYTIGA 250 mg tablets, ZYTIGA 500 mg film-coated tablets, Apalutamide placebo, JNJ-56021927, PREDNISONE, -
Pharma Mar S.A.
Castration-Resistant Prostate Cancer
1 trial -
Zometa 4 mg/100 ml solution for infusion
Cancer Prevention Pharma (Ireland) Limited
High grade osteosarcoma
1 trial -
[18F]MNI-659
Pari Pharma GmbH
Patients with symptomatic and pre-symptomatic Huntington's disease
1 trial -
cagrilintide semaglutide, cagrilintide semaglutide, cagrilintide semaglutide, cagrilintide semaglutide, Placebo + Placebo, cagrilintide semaglutide
Novo Nordisk A/S
Overweight and obesity and type 2 diabetes
1 trial -
coramitug C 10035, liquid dosage form in 20 mL vials with 11 extractable volume
Novo Nordisk A/S
Variant or wild-type transthyretin (TTR) amyloid cardiomyopathy
1 trial -
elafibranor, Elafibranor Placebo
Ipsen Pharma
Primary Biliary Cholangitis (PBC)
1 trial -
elafibranor, Placebo tablet
Ipsen Pharma
Primary Biliary Cholangitis
1 trial -
lactose monohydrate - 100,00 mg/tablet cellulose microcrystalline - 95,60 mg/tablet Croscarmellose sodium - 2,00 mg/tablet Magnesium stearate - 2,40 mg/tablet table coating - OPADRY 20A82938 Yellow - COLORCON, Asmenol, 10 mg, tabletki powlekane
COLLEGIUM PHARMACEUTICAL, INC
Ischemia of the lower limbs in the course of obstructive artery disease
1 trial -
mannitol and microcrystalline cellulose, Tolebrutinib
Genzyme Europe B.V.
Primary Progressive Multiple Sclerosis
1 trial -
nalbuphine HCl ER tablets 60 mg BID
Trevi Therapeutics
Uremic Pruritus
1 trial -
rilonacept 160 mg
Regeneron UK Limited
Familial Cold Autoinflammatory Syndrome (FCAS)
1 trial -
ziltivekimab, Placebo (ziltivekimab C)
Novo Nordisk A/S
Heart failure with mildly reduced or preserved ejection fraction and systemic inflammation
1 trial -
ziltivekimab, Ziltivekimab
Novo Nordisk A/S
The medical condition we are investigating is type 1 AMI (STEMI and NSTEMI). Ziltivekimab is a human monoclonal antibody directed against the interleukin-6 (IL-6) ligand, and currently available clinical data support that ziltivekimab once-monthly reduces inflammation as measured by highsensitivity C-reactive protein (hs-CRP). With the recent proof-of-concept that hs-CRP reduction through inhibition of an upstream pathway leads to reduction in cardiovascular events, it is reasonable to expect that similar inhibition of IL-6 with ziltivekimab also reduces CV risk.The aim of the current study is to demonstrate the efficacy and safety of ziltivekimab in reducing the risk of major adverse cardiovascular events when initiated as early as possible in adult patients with ST-elevation and non-ST-elevation myocardial infarction
1 trial -
60 mg PRAX-114 or 40 mg PRAX-114
PRECISION BIOSCIENCES INC
Post-traumatic Stress Disorder
1 trial -
60 mg Prednisone
United Therapeutics Europe Ltd
Airway Inflammation
1 trial -
601
Sunshine Biopharma
Pathological Myopic Choroidal Neovascularization
1 trial -
601 1.25mg
Sunshine Biopharma
Central Retinal Vein Occlusion
1 trial -
608
Sunshine Biopharma
Axial Spondyloarthritis
1 trial -
608 Dose A
Sunshine Biopharma
Ankylosing Spondylitis
1 trial -
609A
Sunshine Biopharma
Sarcoma, Soft Tissue
1 trial -
89Zr-Bevacizumab
Disc Medicine
NF2-related schwannomatosis
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 Pharmaceuticals International AG
Idiopathic Hypersomnia (IH)
1 trial -
A Phase 1/2 Randomized Trial of BMS-986012 in Combination with Platinum and Etoposide as First-line Therapy in Extensive-Stage Small Cell Lung Cancer
Bristol-Myers Squibb / Pfizer EEIG
Extensive-Stage Small Cell Lung Cancer
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 18,156 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