Intelligence Β· Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors β 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 β searchable for business development and competitive intelligence.
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Oral triiodothyronine
Cardiff Oncology
Postoperative; Dysfunction Following Cardiac Surgery
1 trial -
Oxybutinyn Vaginal Ring 4mg
Teva Pharma GmbH
Overactive Bladder
1 trial -
Ozanimod, Ozanimod
Celgene Europe Limited
Moderately to Severely Active Crohn's Disease
1 trial -
Ozanimod, Ozanimod, Ozanimod
Bristol-Myers Squibb Australia Pty Ltd
Moderately to Severely Active Ulcerative Colitis
1 trial -
Ozempic 1 mg solution for injection in pre-filled pen, Semaglutide Placebo, Ozempic 0.5 mg solution for injection in pre-filled pen, Ozempic 0.25 mg solution for injection in pre-filled pen
NovoThirteen
Mild cognitive impairment (MCI) or mild dementia, both of the Alzheimerβs type
1 trial -
Ozempic 1 mg solution for injection in pre-filled pen, Semaglutide placebo, solution for injection in 1.5 mL pre-filled PDS290 pen injector
NovoThirteen
While it is well-established that long-term good glycaemic control will reduce the risk of diabetic retinopathy development and progression, intensification of glycaemic control has also been associated with an initial worsening of diabetic retinopathy. This phenomenon is known as βearly worseningβ. The rationale of this trial is to establish the long-term effects of semaglutide on diabetic retinopathy in subjects with type 2 diabetes (T2D) using validated and standardised ophthalmic assessments. This trial is a post-authorisation safety study (PASS) conducted as a commitment to the European Medicines Agency
1 trial -
PARACETAMOL , Dapirolizumab pegol, Placebo matching dapirolizumab pegol and without active substance, -, DIPHENHYDRAMINE , -, EPINEPHRINE , -, -
Lacuna Pharma Pty Ltd
Systemic lupus erythematosus (SLE)
1 trial -
PCV21
Sanofi Pasteur
Pneumococcal Infections
1 trial -
PEG-Interferon a-2b + Ribavirin
Universal Integrated
Chronic Hepatitis C Infection in HIV-Infected Persons
1 trial -
PEGASPARGASE
Pari Pharma GmbH
This is a prospective, French, multicenter, open-label, design, stratified on the immunophenotypic characterization (B- or T- lineage) and the patient risk group, that aims at evaluating the efficacy and the tolerance of different schedules of pegaspargase in patients from 12 months to less than 18 years newly diagnosed with standard/medium-risk ALL
1 trial -
PEMBROLIZUMAB , Matching placebo, EIK1001 solution for injection 1.0 mg/mL free base equivalent
Eikon Therapeutics
Advanced Melanoma
1 trial -
PENTHROX 99,9%, liquide pour inhalation par vapeur de 3 mL, MORPHINE
Pari Pharma GmbH
Acute Myocardial Infarction
1 trial -
PF-06651600 Induction Dose
Pfizer
Alopecia Areata
1 trial -
PF-07275315 dose 1
Pfizer
Moderate to Severe Chronic Obstructive Pulmonary Disease
1 trial -
PIPERACILLIN AND BETA-LACTAMASE INHIBITOR , NEGABAN 2 g, poudre pour solution injectable/pour perfusion, MEROPENEM ARROW 1 g, poudre pour solution injectable / pour perfusion
Pari Pharma GmbH
patients hospitalized in ICU with ESBL-producing Enterobacteriaceae severe infection
1 trial -
PL1 - Lyophilisate and solvent for solution for injection, sotatercept
Lacuna Pharma Pty Ltd
Pulmonary Arterial Hypertension (PAH)
1 trial -
PL1 - Placebo to match losmapimod tablets are tablets for oral administration and visually match the active losmapimod tablets, 15 mg., Losmapimod
Fulcrum Therapeutics
Facioscapulohumeral Muscular Dystrophy (FSHD)
1 trial -
PLACEBO OF BELIMUMAB, Benlysta 200 mg solution for injection in pre-filled pen.
Pari Pharma GmbH
Adult patients with persistent or chronic immune thrombocytopenia
1 trial -
PLACEBO SOTAGLIFLOZIN, SOTAGLIFLOZIN
LEXICON PHARMACEUTICALS, INC.
Obstructive Cardiomyopathy, Hypertrophic, Non-obstructive Hypertrophic Cardiomyopathy
1 trial -
PREDNISOLONE , Dupixent 300 mg solution for injection in pre-filled syringe, Placebo matching to dupilumab
Lacuna Pharma Pty Ltd
Bullous Pemphigoid
1 trial -
PREDNISOLONE, Placebo for Depemokimab Injection, Placebo for Prednisolone
GlaxoSmithKline
Hypereosinophilic Syndrome (HES)
1 trial -
PREDNISONE, Entyvio 300 mg powder for concentrate for solution for infusion
Takeda
Active Ulcerative Colitis (UC) or Crohn's disease (CD)
1 trial -
PREDNISONE, Entyvio 300 mg powder for concentrate for solution for infusion
Takeda
Moderately to severely active Ulcerative Colitis (UC)
1 trial -
PREDNISONE, Entyvio 300 mg powder for concentrate for solution for infusion, BUDESONIDE
Takeda
Moderately to severely active Crohn's disease (CD)
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 1β3), 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 β 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