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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Placebo of rosuvastatin 10mg (tablet) as produced by Apotheek A15, Rosuvastatin tablet 10mg Apotheek A15
Disc Medicine
Statin-intolerance, High cardiovascular risk (previous cardiovascular disease or familial hypercholesterolemia)
1 trial -
Placebo used in this trial is a foodgrade, redried potato starch. It is a white powder with bland taste and free from objectionable odours. Insoluble in water with a temperature below 50 °C and most organic solvents, solution is slightly hazy. The product is intended for use in food., POTATO STARCH, SODIUM CHLORIDE, AMILORIDE
Disc Medicine
Autosomal Dominant Polycystic Kidney Disease
1 trial -
Placebo: PL1, Pharmaceutical form: Capsule, Route of administration: Oral use, Hydrocortison DMB 20 mg, tabletten
Disc Medicine
Posttraumatic Stress Disorder (PTSD)
1 trial -
Plavix 75 mg film-coated tablets, CARDIOASPIRIN 100 mg Compresse gastroresistenti, CARDIOASPIRIN 100 mg Compresse gastroresistenti, Plavix 300 mg film-coated tablets
Fondazione Telethon ETS
Patients with atrial fibrillation undergoing percutaneous left atrial appendage closure with the Amulet device
1 trial -
Praluent
Regeneron UK Limited
Heterozygous Familial Hypercholesterolemia
1 trial -
Purified Cortophin Gel, 40 U
ANI PHARMACEUTICALS INC
Gout Arthritis
1 trial -
RITALINE L.P. 10 mg, gélule à libération prolongée
Tour Hekla
Attention Deficit Disorder with or without Hyperactivity (ADHD) is a neurodevelopmental disorder characterized by disabling symptoms of inattention and/or hyperactivity-impulsivity beginning before the age of 12 with significant personal, social, academic and/or occupational impact (American Psychiatric Association 2013). This disorder, whose prevalence is around 5% in children and adolescents, affects 2.6% of adults (American Psychiatric Association 2013; Song et al. 2021).
1 trial -
RIVAROXABAN , RIVAROXABAN, RIVAROXABAN
Pari Pharma GmbH
Patients with excessive supraventricular ectopies or short atrial runs (ESVEA) defined as ≥ 1% premature atrial contractions (PAC) /24 hours or any atrial runs ≥ 20 PACs (but shorter than 30 seconds) on a 24-hour Holter ECG monitoring and CHA2DS2VASC score ≥ 3. Patients with any atrial runs ≥ 20 PACs but shorter than 30 seconds on a 15-21 days Holter ECG monitoring and CHA2DS2VASC score ≥ 3 may also be included in the Short-Run trial.
1 trial -
Rabipur Pulver und Lösungsmittel zur Herstellung einer Injektionslösung in einer Fertigspritze Tollwut-Impfstoff (inaktiviert), RABIPUR, poudre et solvant pour solution injectable en seringue préremplie. Vaccin rabique (inactivé)., Rabipur poeder en oplosmiddel voor oplossing voor injectie in een voorgevulde spuit.Rabiësvaccin (geïnactiveerd).
The George Institute
rabies pre-exposure prophylaxis
1 trial -
Raltitrexed
The First People's Hospital of Lianyungang
Head and Neck Squamous Cell Carcinoma
1 trial -
Rapamune 1 mg coated tablets, MYCOPHENOLATE MOFETIL
The George Institute
End-stage kidney disease in Type 1 diabetes, SIROLIMUS VERSUS MYCOPHENOLATE MOFETIL IN SIMULTANEOUS PANCREAS AND KIDNEY TRANSPLANTATION TO EVALUATE THE RISK OF HERNIA
1 trial -
Regiocit solution pour hémofiltration
Pari Pharma GmbH
Adult patients hospitalized in intensive care with an indication of EER with ARC during the stay.
1 trial -
Rivaroxaban 2.5 mg
Second Xiangya Hospital of Central South University
Acute Coronary Syndrome
1 trial -
SINECATECHINS
The George Institute
Anal high-grade squamous intraepithelial lesions (HSIL).
1 trial -
Sodium Chloride 0.9%, Gardasil 9 suspension for injection. Human Papillomavirus 9-valent Vaccine (Recombinant, adsorbed)
Disc Medicine
Vulvar High-Grade Squamous Intraepithelial Lesion (vHSIL)
1 trial -
Sodium Chloride Fresenius Kabi Italia 0.9 % Solution for infusion , DENOSUMAB, Sodium Fluoride (18F) Life Radiopharma 0,1 - 4 GBq/ml solution injectable
Disc Medicine
Fibrous dysplasia/McCune-Albright syndrome
1 trial -
Standard of care plus Epoprostenol infusion for 8 hours (hrs) per day up to 5 days maximum
United Therapeutics Europe Ltd
Frostbite
1 trial -
Subcutaneous HYLENEX (recombinant human hyaluronidase) and Lactated Ringer's solution
HALOZYME THERAPEUTICS, INC.
Dehydration
1 trial -
Subcutaneous Treprostinil
United Therapeutics Europe Ltd
Pulmonary Arterial Hypertension
1 trial -
Subcutaneous depot medroxyprogesterone acetate
Protara Therapeutics
Contraception
1 trial -
Subcutaneous glargine insulin
Lxo Ireland Designated Activity Company
Diabetes Mellitus
1 trial -
Sufentanil
The First People's Hospital of Lianyungang
Arteriovenous Malformation
1 trial -
TACHOSIL GROUP
Takeda
Lymphocele
1 trial -
TRALOKINUMAB, The placebo presentation is a pre-filled syringe containing the same excipients in the same amounts as the IMP.
LEO Pharma A/S
Atopic dermatitis and moderate-to severe atopic hand eczema
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