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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Salbutamol Aldo-Unión 100 microgramos/dosis suspensión para inhalación en envase a presión, Inhalation powder with lactose monohydrate and magnesium stearate, BREO ELLIPTA, Fluticasone furoate and Vilanterol inhalation powder 100 mcg/25 mcg
Sandoz Pty Ltd
Asthma
1 trial -
Seasonale (levonorgestrel and ethinyl estradiol)
Teva Pharma GmbH
Osteopenia
1 trial -
Seasonale [levonorgestrel (LNG)/ethinyl estradiol (EE)]
Teva Pharma GmbH
Healthy
1 trial -
Spironolactone
Takeda
Atrial Fibrillation
1 trial -
Start antiplatelet monotherapy
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Intracerebral Hemorrhage
1 trial -
Suspension of autologous mononuclear cells separated from bone marrow aspirate
The George Institute
diabetic foot syndrome, lower limb ischemia
1 trial -
Temomedac 20 mg hard capsules, Temomedac 5 mg hard capsules, Tirabrutinib, Temomedac 100 mg hard capsules, Truxima 500 mg concentrate for solution for infusion, Truxima 100 mg concentrate for solution for infusion
Lacuna Pharma Pty Ltd
Relapsed/refractory primary central nervous system lymphoma
1 trial -
The placebo for NW-3509 drug product contains blended lactose monohydrate (29.50 mg/caps), microcrystalline cellulose (70.00 mg/caps), and magnesium stearate (0.50 mg/caps) filled into hard gelatin capsules.
Lacuna Pharma Pty Ltd
treatment-resistant schizophrenia (TRS)
1 trial -
The placebo has the same composition as the investigational medicinal product Clinitrat® (6.563+175,4+89,3+23,3) mg/sachet (with the exception of the active substance), is manufactured by the same manufacturer (uni-pharma kleon tsetis pharmaceutical laboratory s.a) and is not sterile., CLINITRAT® (6.563+175,4+89,3+23,3) mg/sachet ή stick, Κόνις για πόσιμο διάλυμα
Lacuna Pharma Pty Ltd
Second line treatment for colonoscopy preparation
1 trial -
Tiratricol
Ultragenyx UK Limited
Monocarboxylate Transporter 8 Deficiency
1 trial -
Tiratricol, Matching placebo (for participants allocated to the placebo group in the Randomized Treatment Period)
Rare Thyroid Therapeutics International AB
Monocarboxylate Transporter 8 (MCT8) deficiency
1 trial -
VINCRISTINE SULFATE, RITUXIMAB, RITUXIMAB, APIXABAN, Golcadomide, PREDNISONE, DOXORUBICIN HYDROCHLORIDE, CYCLOPHOSPHAMIDE MONOHYDRATE, Golcadomide, Golcadomide 0.2 mg capsule, Golcadomide 0.3 mg capsule, Golcadomide 0.4 mg capsule, Golcadomide, Neulasta 6 mg solution for injection, PREDNISOLONE , VINCRISTINE SULFATE
Celgene Europe Limited
High-risk Large B-cell Lymphoma
1 trial -
Vonoprazan
Phathom Pharmaceuticals
Erosive Esophagitis
2 trials -
Vonoprazan
Phathom Pharmaceuticals
Non-Erosive Gastro-Esophageal Reflux Disease
2 trials -
Vonoprazan
Takeda
Healthy Volunteers
1 trial -
Vonoprazan
Takeda
Helicobacter Pylori
1 trial -
Vonoprazan
Phathom Pharmaceuticals
Helicobacter Pylori Infection
1 trial -
Xevinapant (Debio 1143)
Serono Europe Limited
Squamous Cell Carcinoma of the Head and Neck
1 trial -
donor lymphocyte infusion
The First People's Hospital of Lianyungang
Minimal Residual Disease
1 trial -
iron isomaltoside(Monofer®)
Hospital Authority, Hong Kong
Anemia, Iron-Deficiency
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 -
levonorgestrel/EE 0.15/0.03 and EE 0.01 mg tablets
Teva Pharma GmbH
Dysmenorrhea
2 trials -
metronomic adjuvant chemotherapy with capecitabine
Chongqing Claruvis Pharmaceutical Co.,
Nasopharyngeal Cancinoma (NPC)
1 trial -
ziltivekimab, Ziltivekimab
NovoThirteen
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
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