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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Azithromycin 600 mg Tablet
Teva Pharma GmbH
Healthy
2 trials -
BG-60366
BEONE MEDICINES AUS PTY LTD
Non-Small Cell Lung Cancer
1 trial -
BMS-906024
Bristol-Myers Squibb
Cancer
1 trial -
BPX-601
Regeneron UK Limited
Prostate Cancer
1 trial -
BPX-601
Regeneron UK Limited
Metastatic Castration-resistant Prostate Cancer
1 trial -
Bimzelx 320 mg solution for injection in pre-filled pen, Bimzelx 160 mg solution for injection in pre-filled syringe, Bimzelx 160 mg solution for injection in pre-filled syringe, Bimzelx 160 mg solution for injection in pre-filled pen, Bimzelx 160 mg solution for injection in pre-filled pen, Bimzelx 160 mg solution for injection in pre-filled syringe, Bimzelx 320 mg solution for injection in pre-filled syringe, Bimzelx 160 mg solution for injection in pre-filled pen, Bimzelx 160 mg solution for injection in
Lacuna Pharma Pty Ltd
Hidradenitis suppurativa, Axial spondyloarthritis, Moderate to Severe Plaque Psoriasis, Psoriatic arthritis
1 trial -
Bioequivalence of One Tablet of Gliclazide MR 120 mg (S005190) and Two Tablets of Gliclazide MR 60 mg (Diamicron® MR) in Healthy Participants under Fasting Conditions.
The George Institute
No medical condition.
1 trial -
Bioequivalence of One Tablet of Gliclazide MR 120 mg (S005190) and Two Tablets of Gliclazide MR 60 mg (Diamicron® MR) in Healthy Participants under Fed Conditions.
The George Institute
No medical condition.
1 trial -
Bioequivalence of One Tablet of Gliclazide MR 90 mg (S005190) and One and a Half Tablets of Gliclazide MR 60 mg (Diamicron® MR) in Healthy Participants under Fed Conditions.
The George Institute
No medical condition.
1 trial -
C6001001 - A Study to Learn about the Study Medicine PF-08052667 in People with Bladder Cancer.
Pfizer Australia Pty Ltd
Non-muscle invasive bladder cancer (NMIBC)
1 trial -
C6081001: A Phase 1 Study of PF-07985045 in Participants with Advanced Solid Tumors
Pfizer Australia Pty Ltd
KRAS mutated advanced solid tumors
1 trial -
CITY
Pari Pharma GmbH
Cutaneous T-cell lymphomas (CTCL)
1 trial -
CSL760
CSL Behring GmbH
Coronavirus Disease 2019 (COVID-19)
1 trial -
Cardiovascular safety assessment of Tanimilast in healthy volunteers
Chiesi Farmaceutici S.p.A
This is Phase I study to assess the effect on the heart rate (HR) and cardiovascular safety according to electrocardiographic monitoring (including QT and QTc intervals) of CHF6001(Tanimilast) administered with NEXThaler® device in healthy adult volunteers.
1 trial -
Comparative Bioavailability of Levonorgestrel 52 mg Intrauterine System versus Mirena® in Healthy Pre-Menopausal, Non-Pregnant Female Participants.
Laboratorios Tillomed Spain S.L.U
No medical condition.
1 trial -
Dose of 60 mg/kg Fraction IV-1 Alpha1-Proteinase Inhibitor
Takeda
Alpha 1-Antitrypsin Deficiency
1 trial -
Drug 601
Sunshine Guojian Pharmaceutical (Shanghai) Co.,
Diabetic Macular Edema
1 trial -
Drug 601
Sunshine Guojian Pharmaceutical (Shanghai) Co.,
Wet Age-related Macular Degeneration
1 trial -
E6007
Eisai Co.,
Healthy Volunteers
1 trial -
EXT608
Universal Integrated
Safety Issues
1 trial -
Effect of Erythromycin on the absorption, metabolism and elimination of CHF6001 in healthy volunteers
Chiesi Farmaceutici S.p.A
This study is a phase I trial to investigate the effect of inhibition of CYP3A4/5 by Erythromycin on the pharmacokinetics of CHF6001 in healthy volunteers.
1 trial -
Evaluation of bioequivalence of two products containing 600 mg ibuprofen: Ibuprofen Sopharma 600 mg film-coated tablets (Test) vs. Brufen 600 mg film-coated tablets (Comparator). A monocentric, open, randomized, single dose, two-period, crossover trial in healthy volunteers
Lacuna Pharma Pty Ltd
No therapeutic indication in the current trial with healthy volunteers.
1 trial -
FHD-609
Foghorn Therapeutics
Advanced Synovial Sarcoma
1 trial -
FTX-6058/placebo oral capsule(s)
Fulcrum Therapeutics
Healthy Adult Subjects
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