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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Amlitelimab, Placebo, -, TACROLIMUS , PIMECROLIMUS , Amlitelimab
Sanofi-aventis Healthcare Pty Ltd
Dermatitis atopic
1 trial -
Amlitelimab, Placebo, Amlitelimab, PIMECROLIMUS , -, TACROLIMUS
Sanofi-aventis Healthcare Pty Ltd
atopic dermatitis
1 trial -
Amlodipine
United Therapeutics Europe Ltd
Depression
1 trial -
Amlodipine
The First People's Hospital of Lianyungang
Sleep Apnea Syndrome
1 trial -
Amoxycillin
United Therapeutics Europe Ltd
Non-Severe Pneumonia With Wheeze
1 trial -
Amvuttra 25 mg solution for injection in pre-filled syringe
Alnylam Netherlands B.V.
Transthyretin Amyloidosis with Cardiomyopathy (ATTR Amyloidosis with Cardiomyopathy)
1 trial -
Amvuttra 25 mg solution for injection in pre-filled syringe, Onpattro 2 mg/mL concentrate for solution for infusion.
Alnylam Netherlands B.V.
Hereditary Transthyretin Amyloidosis
1 trial -
Amyvid 1900 MBq/mL solution for injection, VIZAMYL 400 MBq/mL solution for injection, Amyvid 800 MBq/mL solution for injection, VIZAMYL 400 MBq/mL solution for injection, Trontinemab, Placebo Trontinemab, Amyvid 800 MBq/mL solution for injection, Neuraceq 300 MBq/mL solution for injection, Amyvid 1900 MBq/mL solution for injection, [18F]MK-6240
Hoffmann-La Roche
Early Symptomatic Alzheimer’s Disease (MCI to Mild Dementia due to AD)
1 trial -
An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome
CORCEPT THERAPEUTICS INC
Endogenous Cushing Syndrome
1 trial -
An Open-Label Roll-Over Study to Evaluate the Long-Term Safety and Efficacy of DCR-PHXC Solution for Injection (subcutaneous use) in Patients with Primary Hyperoxaluria
Lacuna Pharma Pty Ltd
Primary Hyperoxaluria
1 trial -
An open label, single arm, extension trial to examine long-term safety of Iclepertin once daily in patients with schizophrenia who have completed previous Iclepertin Phase III trials.(CONNEX-X)
Boehringer Ingelheim
Schizophrenia
1 trial -
Anagrelide Hydrochloride
Takeda
Essential Thrombocythemia (ET)
1 trial -
Anakinra 100mg and Placebo Depo-Medrone
United Therapeutics Europe Ltd
Gout
1 trial -
Anastrozole
United Therapeutics Europe Ltd
Breast Cancer
2 trials -
Angoron 150 mg/3 ml amp ενέσιμο διάλυμα, FLECARDIA Διάλυμα για ένεση/έχχυση
Lacuna Pharma Pty Ltd
Cardioversion of paroxysmal atrial fibrillation in the Emergency Department in patients with coronary artery disease without residual ischemia and an left ventricular ejection fraction > 35%
1 trial -
Anifrolumab
AstraZeneca
Active Systemic Lupus Erythematosus
3 trials -
Anifrolumab
AstraZeneca
Cutaneous Lupus Erythematosus
1 trial -
Anifrolumab
AstraZeneca AB
Moderate-to-severe Systemic Lupus Erythematosus (SLE)
1 trial -
Anifrolumab
AstraZeneca
Systemic Lupus Erythematosus
1 trial -
Anifrolumab, Matching placebo solution for injection in aPFS; 0.8 mL fill volume
AstraZeneca AB
Cutaneous Lupus Erythematosus
1 trial -
Anodal tDCS
United Therapeutics Europe Ltd
Stroke
1 trial -
Anti C5 Complement mAb Placebo, Ultomiris 300 mg/30 mL concentrate for solution for infusion
Alexion Europe SAS
Hematopoietic stem cell transplant-associated thrombotic microangiopathy
1 trial -
Antihemophilic Factor (Recombinant) - Plasma/Albumin Free Method
Baxalta Innovations GmbH
Hemophilia A
1 trial -
Antihemophilic Factor (Recombinant), Porcine Sequence (BAX 802)
Takeda
Hemophilia A
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