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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KEYTRUDA 25 mg/mL concentrate for solution for infusion, PRT3789
Prelude Therapeutics Inc
non-small cell lung cancer (NSCLC), Esophageal Cancer, Advanced or Metastatic Solid Tumors with a SMARCA4 Mutation
1 trial -
KEYTRUDA 25 mg/mL concentrate for solution for infusion., Darleukin, Fibromun
Philogen S.p.A.
Patients with diagnosis of unresectable clinical stage III or IV metastatic melanoma, with presence of injectable cutaneous, subcutaneous or nodal lesions and resistant to or progressing upon anti-PD1 immunotherapy
1 trial -
KEYTRUDA 25 mg/mL concentrate for solution for infusion., LIBTAYO 350 mg concentrate for solution for infusion.
Ningbo Cancer Hospital
METAREM:Patients with advanced cancer, as defined as unresectable locally advanced malignancies or metastatic cancers (including leukemias and lymphomas). META-1: Patients in first-line therapy for advanced metastatic NSCLC with PD-L1 Tumor Proportion Score (TPS) >50%, without EGFR/ ALK/ ROS1 mutations and irrespective of their histological subtype (squamous or non-squamous)
1 trial -
KPT-8602
Karyopharm Therapeutics Inc
Relapsed/Refractory Multiple Myeloma (RRMM)
1 trial -
KT-621
Kymera Therapeutics
Eosinophilic Asthma
1 trial -
KT-621
Kymera Therapeutics
Atopic Dermatitis
2 trials -
KT-621, KT-621, KT-621, The placebo is used in the Double-blind, Placebo-controlled (DBPC) Treatment Period. Participants are randomly assigned to receive either KT-621 or a matching placebo. The placebo is designed to match the study drug in appearance and administration method to maintain blinding.
Kymera Therapeutics
Moderate to Severe Atopic Dermatitis
1 trial -
KT-621, Placebo oral tablet matched to KT-621, KT-621, KT-621
Kymera Therapeutics
Uncontrolled Moderate to Severe Eosinophilic Asthma
1 trial -
KYV-101
Kyverna Therapeutics
Systemic Sclerosis
1 trial -
KYV-101
Kyverna Therapeutics
Multiple Sclerosis, Primary Progressive
1 trial -
KYV-101 anti-CD19 CAR-T cell therapy
Kyverna Therapeutics
Lupus Nephritis
2 trials -
KYV-101, an autologous fully-human anti-CD19 CAR T-cell immunotherapy
Kyverna Therapeutics
ANCA-IgG-positive ANCA Associated Vasculitis
1 trial -
KYV101
Kyverna Therapeutics
Rheumatoid Arthritis
1 trial -
Kesimpta 20 mg solution for injection in pre-filled pen, Ocrevus 300 mg concentrate for solution for infusion, MabThera 500 mg concentrate for solution for infusion, MabThera 100 mg concentrate for solution for infusion, MabThera 100 mg concentrate for solution for infusion, Kesimpta 20 mg solution for injection in pre-filled syringe, Ocrevus 300 mg concentrate for solution for infusion, Kesimpta 20 mg solution for injection in pre-filled syringe, Ocrevus 300 mg concentrate for solution for infusion, MabThe
Kyverna Therapeutics
Primary or Secondary Progressive Multiple Sclerosis
1 trial -
Ketamine
Grace Therapeutics
Obstetric Pain
1 trial -
L-citrulline
United Therapeutics Europe Ltd
Post Deployment Related Asthma
1 trial -
LAAM
BRIGHT MINDS BIOSCIENCES INC.
Behavior Therapy
1 trial -
LAD328, SODIUM CHLORIDE
Almirall, S.A.
moderate-to-severe hidradenitis suppurativa
1 trial -
LEAn Body Mass Normalization of OXaliplatin Based Chemotherapy
The George Institute
Colon cancer
1 trial -
LENOGRASTIM , RITUXIMAB, BUSULFAN , FLUDARABINE , PLERIXAFOR , OTL-203
Orchard Therapeutics (Netherlands) B.V.
Mucopolysaccharidosis type I Hurler
1 trial -
LENVATINIB, KEYTRUDA 25 mg/mL concentrate for solution for infusion.
Disc Medicine
high risk or poor response after chemoradiation and brachytherapy for locally advanced cervix cancer
1 trial -
LEVOFOLINATE DE CALCIUM ZENTIVA 10 mg/ml, solution injectable (IM/IV), Docetaxel Accord 20 mg/1 ml concentrate for solution for infusion, Bemarituzumab, FLUOROURACILE ACCORD 50 mg/ml, solution Γ diluer pour perfusion, OXALIPLATINE ACCORD 5 mg/ml, solution Γ diluer pour perfusion
CERO THERAPEUTICS HOLDINGS, INC.
gastric and gastro-oesophageal junction adenocarcinomas
1 trial -
LN-145
Iovance Biotherapeutics B.V.
Non Small Cell Lung Cancer
1 trial -
LN-145
Iovance Biotherapeutics B.V.
Squamous Cell Carcinoma of the Head and Neck
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