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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Study of EGF816 in combination with selected targeted agents in EGFR-mutant NSCLC.
Novartis Pharmaceuticals
Patients with EGFR-mutant Non Small Cell Lung Cancer
1 trial -
Study of MK-4830 as Monotherapy and in Combination With Pembrolizumab (MK-3475) in Participants With Advanced Solid Tumors (MK-4830-001)
Merck Sharp and Dohme
Advanced Pancreatic cancer, Unresectable Glioblastoma and Variants, PD-1-exposed Advanced/Met HNSCC, Advanced/Met HNSCC, Advanced/Met NSCLC, Advance/Met RCC, Advanced/Met Gastric or GEJ adenocarcinoma, Ovarian Cancer. TNBC, Advanced Mesothelioma, Advanced Solid tumors(coformulation)
1 trial -
Study of safety and efficacy of DKY709 alone or in combination with PDR001 in patients with advanced solid tumors.
Novartis Pharmaceuticals
Nasopharyngeal Carcinoma, Triple Negative Breast Cancer, Microsatellite Stable Colorectal Cancer, Non-Small Cell Lung Cancer, Cutaneous Melanoma
1 trial -
Study of safety and preliminary efficacy of VAY736 given alone or in combination with other antineoplastic agents in patients with NHL
Novartis Pharmaceuticals
Relapsed/refractory Non Hodgkin Lymphoma
1 trial -
Vaccine/device combination for prevention of HFRS
United Therapeutics Europe Ltd
Hemorrhagic Fever With Renal Syndrome
1 trial -
Valemetostat Tosylate, DS-8201a, Datopotamab deruxtecan, Valemetostat Tosylate, Valemetostat Tosylate
Daiichi Sankyo
This study will be a Phase 1b, global, multicenter, open-label, 2-part study of valemetostat in combination with DXd ADCs. The Master Protocol study design contains independent subprotocols, which have been defined by treatment combination and subject population, as follows: Sub-protocol A: Valemetostat in combination with T-DXd in subjects with previously treated, unresectable and/or metastatic HER2-low (immunohistochemistry[IHC] 1+ or IHC 2+/in situ hybridization [ISH]-negative) BC; for details, see Sub-protocol A. Sub-protocol B: Valemetostat in combination with T-DXd in subjects with previously treated, advanced or metastatic HER2-positive gastric or GEJ adenocarcinoma; for details, see Sub-protocol B. Sub-protocol C: Valemetostat in combination with Dato-DXd in subjects with previously treated, locally advanced, unresectable, or metastatic non-squamous NSCLC with or without actionable genomic alteration(s); for details, see Sub-protocol C.
1 trial -
WX-UK1 in combination with Capecitabine
United Therapeutics Europe Ltd
Advanced Malignancies
1 trial -
tasimelteon
Vanda Pharmaceuticals Netherlands B.V.
Pharmacodyamics and Pharmacokinetics of Tasimelteon Alone and in Combination With Ethanol
1 trial -
ββAMG 436 as monotherapy and combination therapy in participants with Microsatellite Instability-High/Mismatch Repair Deficient Solid Tumors β
Amgen
microsatellite instability high/mismatch repair deficient (MSI-H/dMMR) solid tumors
1 trial -
βINSIGHTβ An explorative, open-labeled, phase I trial to evaluate feasibility and safety of eftilagimod alpha (IMP321, a LAG-3Ig fusion protein acting as LAG-3 agonist) in combination with immunotherapeutic, targeted or chemotherapeutic agents or when administered via new routes of application in advanced stage solid tumors
The George Institute
Histologically confirmed locally advanced or metastatic solid tumor (Strata A, B, D): Specification for Stratum C: Only patients with NSCLC adenocarcinomas, (squamous or adenosquamous not permitted) who are scheduled to receive platin + pembrolizumab + pemetrexed standard treatment (only for Stratum C) Specification for Stratum E: Including only metastatic or irresectable locally advanced urothelial carcinomas (only for Stratum E)
1 trial -
Amlodipine besylate/atorvastatin calcium single pill combination
Pfizer
Hypertension
1 trial -
Artemether-lumefantrine combination
United Therapeutics Europe Ltd
Plasmodium Vivax Infection
1 trial -
Artesunate-amodiaquine combination
United Therapeutics Europe Ltd
Malaria,Falciparum
1 trial -
COMBINATIONS
Disc Medicine
muscle protein turnover hemodialysis
1 trial -
Coartemβ’ (Artemether-lumefantrine combination)
United Therapeutics Europe Ltd
Malaria
1 trial -
Combination Cinacalcet with Vitamin D analogue
Hospital Authority, Hong Kong
Secondary Hyperparathyroidism
1 trial -
Combination NRT (Nicotine patch, Nicotine lozenge)
BRIGHT MINDS BIOSCIENCES INC.
Smoking Cessation
1 trial -
Combination of antiplatelet drugs and anticoagulants for at least one month
The First People's Hospital of Lianyungang
Acute Myocardial Infarction
1 trial -
Dexmedetomidine-esketamine combination
The First People's Hospital of Lianyungang
Obstructive Sleep Apnea
1 trial -
Glycopyrronium in Combination With Tropisetron
The First People's Hospital of Lianyungang
Postoperative Nausea and Vomiting
1 trial -
Harvoni (Fixed dose combination ledipasvir/sofosbuvir)
BRIGHT MINDS BIOSCIENCES INC.
Hepatitis C
1 trial -
Prothrombin complex concentrate (coagulation factors IX, II, VII and X in combination)
Takeda
Prothrombin Complex Factor Deficiency
1 trial -
Triple combination therapy group
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Type 2 Diabetes Mellitus
1 trial -
brinzolamide 1%/brimonidine 0.2% fixed combination
Novartis Pharmaceuticals
Glaucoma
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