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.
-
ABBV-RGX-314 or RGX-314, ABBV-RGX-314 or RGX-314, Lucentis 10 mg/ml solution for injection in pre-filled syringe, Eylea 40 mg/mL solution for injection in pre-filled syringe
AbbVie Deutschland GmbH & Co. KG
Neovascular age-related macular degeneration
1 trial -
ABIRATERONE ACETATE, ABIRATERONE ACETATE, ENZALUTAMIDE, ABIRATERONE ACETATE, Pluvicto 1 000 MBq/mL solution for injection/infusion, Locametz 25 micrograms kit for radiopharmaceutical preparation, ENZALUTAMIDE, ENZALUTAMIDE
Novartis Pharmaceuticals
PSMA-positive metastatic castration-resistant prostate cancer
1 trial -
ABIRATERONE ACETATE, DAROLUTAMIDE, Locametz 25 micrograms kit for radiopharmaceutical preparation, APALUTAMIDE, Pluvicto 1 000 MBq/mL solution for injection/infusion, ENZALUTAMIDE
Ningbo Cancer Hospital
Novo metastatic hormone-sensitive prostate cancer (mHSPC) patients having a serum PSA level of ≥ 0.2 ng/mL at 6 to 8 months after systemic treatment initiation for mHSPC (i.e. poor responders) in the absence of evidence of cancer progression (including a rising PSA level)
1 trial -
ACICLOVIR VIATRIS 500 mg, poudre pour solution injectable (I.V.), CHLORURE DE SODIUM 0,9 % B. BRAUN, solution injectable en ampoule
Pari Pharma GmbH
Patients in ICU with invasive mechanical ventilation and HSV throat reactivation with 1 or no organ failures.
1 trial -
ACIDE FOLIQUE CCD 5 mg, comprimé, PLACEBO D'ASPIRINE PROTECT, ASPIRINE PROTECT 100 mg, comprimé gastro-résistant, PLACEBO D'ACIDE FOLIQUE
Pari Pharma GmbH
Patients presenting to ENT emergencies with a unilateral sudden sensorineural hearing loss (SSNHL). SSNHL is defined according to the American ENT society guidelines criteria as a subset of SSNHL that is sensorineural in nature, occurs within a 72 hour window, and consists of a decrease in hearing of ≥30 decibels affecting at least 3 consecutive frequencies: 1. A history of an idiopathic and unilateral sudden decrease in hearing > 72 hours and <15 days. 2. A unilateral sensorineural hearing loss demonstrable on a pure‐tone audiogram at the time of entry into the trial. 3. No other neurological signs except the eight cranial nerve defect; no other types of hearing loss as conductive forms of hearing impairment. 4. No history of fluctuating sensorineural hearing loss or otologic disease.
1 trial -
ACTILYSE 50mg placebo, ACTILYSE, poudre et solvant pour solution injectable et perfusion
Pari Pharma GmbH
intermediate-high-risk acute pulmonary embolism
1 trial -
ACTILYSE, poudre et solvant pour solution injectable et perfusion, ACTILYSE, poudre et solvant pour solution injectable et perfusion, Metalyse 10,000 units powder and solvent for solution for injection, ACTILYSE, poudre et solvant pour solution injectable et perfusion, Metalyse 5 000 units (25 mg) powder for solution for injection
Tour Hekla
Acute ischaemic stroke due to basilar artery occlusion.
1 trial -
ACTIQ (Oral transmucosal fentanyl citrate)
Teva Pharma GmbH
Breakthrough Pain
1 trial -
ACTISOUFRE, solution pour pulvérisation nasale/buccale en flacon pressurisé, Actisoufre Placebo
Laboratoire HRA Pharma
rhinosinusitis not requiring antibiotic therapy, rhinopharyngitis not requiring antibiotic therapy, Acute rhinitis not requiring antibiotic therapy
1 trial -
ADVATE 500 IU powder and solvent for solution for injection., VEYVONDI 1300 IU powder and solvent for solution for injection., ADVATE 1000 IU powder and solvent for solution for injection., VEYVONDI 650 IU powder and solvent for solution for injection.
Takeda
severe von Willebrand Disease
1 trial -
ADX-102 Ophthalmic Solution (0.5%)
Aldeyra Therapeutics
Non-infectious Anterior Uveitis
1 trial -
AIN457
Novartis Pharmaceuticals
Non-infectious Uveitis
1 trial -
AK112 Injection
Summit Therapeutics
Non-Squamous Non-small Cell Lung Cancer
1 trial -
ALN-TTRSC04, Amvuttra 25 mg solution for injection in pre-filled syringe
Alnylam Netherlands B.V.
Hereditary transthyretin-mediated amyloidosis with polyneuropathy
1 trial -
ALTUVOCT 2 000 IU powder and solvent for solution for injection, ALTUVOCT 3 000 IU powder and solvent for solution for injection, ALTUVOCT 4 000 IU powder and solvent for solution for injection, ALTUVOCT 250 IU powder and solvent for solution for injection, ALTUVOCT 1 000 IU powder and solvent for solution for injection, ALTUVOCT 500 IU powder and solvent for solution for injection
Swedish Orphan Biovitrum AB (publ)
Haemophilia A
1 trial -
ALVAC-HIV vCP1521 + AIDSVAX
United Therapeutics Europe Ltd
HIV Infection
1 trial -
ALXN1850, Strensiq 40 mg/ml Solution for Injection, Strensiq 100 mg/ml Solution for Injection
Alexion Europe SAS
Hypophosphatasia
1 trial -
AMG 133, Placebo for AMG 133, AMG 133, AMG 133
Amgen
"Moderate to severe obstructive sleep apnea (OSA) in adults living with overweight or obesity"
1 trial -
ARALAST NP 60 mg/kg
Takeda
Chronic Obstructive Pulmonary Disease
1 trial -
ARGX-113, Vyvgart 20 mg/mL concentrate for solution for infusion, Vyvgart 1 000 mg solution for injection
argenx
Generalized Myasthenia Gravis
1 trial -
ARO-APOC3 PFS, ARO-APOC3, 0.9% Normal Saline for injection
Arrowhead Pharmaceuticals Ireland Limited
Familial Chylomicronemia Syndrome (FCS)
1 trial -
ARO-APOC3 PFS, Plozasiran Injection Placebo
Arrowhead Pharmaceuticals Ireland Limited
Hypertriglyceridemia
1 trial -
ARO-APOC3 PFS, Plozasiran Injection Placebo
Arrowhead Pharmaceuticals Ireland Limited
Severe hypertriglyceridemia (SHTG)
1 trial -
ASP8951, Sodium Chloride 0.9% Intravenous Infusion BP
Astellas Pharma GmbH
Claudin (CLDN)18.2-Positive, HER2-Negative, Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma
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