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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91-day Levonorgestrel Oral Contraceptive
Teva Pharma GmbH
Bone Mineral Density
1 trial -
A Clinical Trial for Patients with Advanced Cancers
Corbus Pharmaceuticals Holdings
Advanced Solid tumour
1 trial -
A Phase 1/2 Dose Escalation Study of CRN09682 With an Expansion Phase in Participants with Progressive Metastatic Somatostatin Receptor Type 2 (SST2)-Expressing Neuroendocrine Neoplasms (NENs) and Other SST2-Expressing Solid Tumors
Lacuna Pharma Pty Ltd
Metastatic or locally advanced SST2-positive neuroendocrine neoplasms in adults
1 trial -
A Phase 1/2, Multicenter, Open-Label Study to Determine the Safety, Pharmacokinetics, and Pharmacodynamics of DNL310 in Pediatric Participants with Hunter Syndrome
Denali Therapeutics
Hunter Syndrome (Mucopolysaccharidosis Type II [MPS II])
1 trial -
A Phase 1/2, Multicenter, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Exploratory Efficacy of Intrathecally Administered Gene Therapy AMT-162 in Adult Participants with SOD1 Amyotrophic Lateral Sclerosis (SOD1-ALS)
uniQure biopharma B.V.
Amyotrophic Lateral Sclerosis (ALS)
1 trial -
A Phase 1/2, Open-label Study Evaluating the Efficacy, Safety, and Pharmacokinetics (PK) of Luveltamab Tazevibulin (STRO-002) in Infants and Children < 12 years of age with CBFA2T3::GLIS2 Acute Myeloid Leukemia (AML)
SUTRO BIOPHARMA, INC.
Acute Myeloid Leukemia (AML)
1 trial -
A Phase 1/2a, First in Human, Open-Label, Multicenter, Dose Escalation Study with Expansion Cohorts to Evaluate the Safety, Tolerability, and Preliminary Activity of LB101 in Subjects with Advanced Solid Tumors
Centessa Pharmaceuticals plc
Advanced solid tumors
1 trial -
A Phase 2 Open-Label Study to Evaluate the Safety and Efficacy of DCR-PHXC in Patients With Primary Hyperoxaluria Type 1 and Severe Renal Impairment, With or Without Dialysis
Lacuna Pharma Pty Ltd
Primary Hyperoxaluria
1 trial -
A Phase 2, Multiple Ascending Dose, Open-label, Proof-of-concept Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Activity of HM15136 Treatment for 8 Weeks in Subjects Aged β₯2 Years With Congenital Hyperinsulinism (CHI) (ACHIEVE)
Alphapharm Pty Ltd
Congenital Hyperinsulinism (CHI)
1 trial -
A Phase 2, Randomized, Parallel, Open-Label Study to Investigate the Safety, Efficacy, and Pharmacokinetics of Various Dosing Regimens of Single-Agent Belantamab Mafodotin (GSK2857916) in Participants with Relapsed or Refractory Multiple Myeloma (DREAMM-14)
GlaxoSmithKline
Multiple Myeloma
1 trial -
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Clinical Activity of GSK5733584 for Injection in Subjects with Advanced Solid Tumors
GlaxoSmithKline
Ovarian Neoplasms
1 trial -
A Phase I, open-label, multi-center exploratory safety and efficacy study with PSMA, SSTR2 and GRPR targeted radioligand therapy in metastatic neuroendocrine prostate cancer
Novartis Pharmaceuticals
Metastatic neuroendocrine prostate cancer
1 trial -
A Phase I/II open label study to assess safety and preliminary evidence of a therapeutic effect of Azeliragon combined with conventional concurrent radiation and temozolomide in patients with newly diagnosed glioblastoma.
Lacuna Pharma Pty Ltd
Glioblastoma
1 trial -
A Phase II Multicenter, Open-Label Study to evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Pediatric Patients with Duchenne Muscular Dystrophy (SHIELD DMD)
Hoffmann-La Roche
Duchenne Muscular Dystrophy (DMD)
1 trial -
A Phase II, Single-Arm, Open-Label Study Evaluating the Safety and Pharmacokinetics of the Intravenous FixedβDose Combination (IV FDC) of Tiragolumab and Atezolizumab in Participants with Locally Advanced, Recurrent or Metastatic Solid Tumors
Hoffmann-La Roche
Solid Tumors
1 trial -
A Phase II, multi-site, open-label, dose-titration trial to investigate the safety, tolerability, pharmacokinetics, and efficacy of Lu AG13909 in adults with Cushingβs disease
H. Lundbeck A/S
Cushing's Disease
1 trial -
A phase 2 trial assessing Ifenprodil as a ReMyelinating repurpOsed Drug in Multiple Sclerosis β MODIF-MS
Pari Pharma GmbH
Multiple sclerosis
1 trial -
A sterile preservative-free solution with identical composition as the drug product, but without the protein.
Kiniksa Pharmaceuticals International, plc
SjΓΆgrenβs Disease
1 trial -
A-623
Santhera Pharmaceuticals (Deutschland) GmbH
Systemic Lupus Erythematosus
1 trial -
A006
Amphastar France Pharmaceuticals
Asthma
1 trial -
A006 DPI
Amphastar France Pharmaceuticals
Asthma
2 trials -
AB-729
Arbutus Biopharma Corp
Chronic Hepatitis b
1 trial -
ABC294640
RedHill Biopharma
Cholangiocarcinoma
1 trial -
ABIRATERONE, DAROLUTAMIDE, DZR123, -, -, ABIRATERONE, DZR123, DAROLUTAMIDE
Novartis Pharmaceuticals
Metastatic hormone-sensitive prostate cancer
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