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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A Study to evaluate the effect of a high-fat meal on the Pharmacokinetics of the Selective MET kinase Inhibitor DO-2 in subjects in good health
Wuhan Createrna Science and Technology Co., Ltd
Healthy volunteer
1 trial -
A Study to find out the safety, tolerability and interaction of drug with body (including the effect of Itraconazole on RO7268489) and also what the body does to RO7268489 after oral intake by healthy participants
Hoffmann-La Roche
Not applicable
1 trial -
A Study to see how safe is RO7567132 as Single Agent and in Combination with Atezolizumab, how the body gets rid of it and how effective it is in people with Advanced and/or Metastatic Solid Tumors
Hoffmann-La Roche
Advanced and/or Metastatic Solid Tumors
1 trial -
A TWO-PART ABSOLUTE BIOAVAILABILITY STUDY DESIGNED TO EVALUATE THE PHARMACOKINETIC PROFILE OF VELUSETRAG FOLLOWING SINGLE-DOSE ADMINISTRATION OF INTRAVENOUS AND ORAL CAPSULE FORMULATIONS IN HEALTHY MALE AND FEMALE SUBJECTS
Alfasigma S.p.A.
chronic intestinal pseudo-obstruction (CIPO)
1 trial -
A Trial to Determine if Quabodepistat is Processed Differently in Adults with Reduced Liver Function Compared to Adults with Normal Liver Function
Otsuka Beijing Research Institute
Tuberculosis
1 trial -
A Trial to Examine the Effects of MSP-2020 on Brain Activity in Healthy Adults
Otsuka Beijing Research Institute
Incomplete Response - Major Depressive Disorder (IR-MDD)
1 trial -
A bioavailability study of epinephrine following a single dose of emergency response auto-injector in comparison to epinephrine injection into muscle via syringe in healthy adults.
Mylan Pharma UK
Allergic reactions (Type 1), including anaphylaxis, idiopathic anaphylaxis or exercise-induced anaphylaxis
1 trial -
A clinical study of MK-1289 in healthy adult men (MK-1289-001)
Merck Sharp and Dohme
COVID-19 Infection
1 trial -
A clinical study of MK-3508 in healthy people (MK-3508-006)
Merck Sharp and Dohme
Respiratory syncytial virus infection
1 trial -
A clinical study of MK-4646 in healthy people (MK-4646-002)
Merck Sharp and Dohme
HIV infection
1 trial -
A clinical study of MK-4646 in people with HIV (MK-4646-003)
Merck Sharp and Dohme
HIV infection
1 trial -
A clinical trial investigating the safety and biological activity of the antibody BNT351 in adults living without and with HIV
BioNTech SE
HIV-1 infection
1 trial -
A clinical trial of MK-1824 in healthy participants (MK-1824-001)
Merck Sharp and Dohme
Heart failure with preserved ejection fraction
1 trial -
A clinical trial to learn how liver function affects the blood levels of DAK539 in people with advanced cancer
Novartis Pharmaceuticals
Advanced Malignancies and Hepatic Impairment
1 trial -
A dose-finding Phase I study of F8IL10 intra-articular treatment in Rheumatoid Arthritis
Philogen S.p.A.
Patients with Rheumatoid Arthritis (RA) who, despite treatment with stable doses (for at least 3 months) of disease-modifying antirheumatic drugs (DMARDs, conventional, biologic and/or targeted synthetic), present arthritis flare(s) suitable for intra-articular (IA) injection in a knee, shoulder, ankle, wrist or elbow.
1 trial -
A drug-drug interaction trial in healthy female participants to investigate the effect of aprocitentan on combined hormonal contraceptives.
Lacuna Pharma Pty Ltd
Not applicable - healthy volunteer trial
1 trial -
A first-in-human trial to evaluate safety, tolerability, and pharmacokinetics of single and multiple oral doses of Debio 1453P in healthy adults
Alphapharm Pty Ltd
Sexual Transmitted Infection (STI)
1 trial -
A first-in-human, randomized, participant and investigator blinded, placebo-controlled single and multiple ascending dose study to assess the safety, tolerability and pharmacokinetics of HJB647 in healthy participants and otherwise healthy participants with elevated blood pressure, with an open-label CYP3A inhibitor drug-drug interaction part
Novartis Pharmaceuticals
Heart failure (HF)
1 trial -
A multicentric, open-label, non-randomized study to evaluate the pharmacokinetic, safety and tolerability of ITF2357 given as an oral single 50 mg dose in participants with chronic hepatic impairment relative to matched participants with normal hepatic function.
Italfarmaco S.p.A.
Participants with normal hepatic function, Participants with moderate HI, Participants with mild HI
1 trial -
A phase 1 study of FluBHPVE6E7 immunotherapy in patients with HPV16-associated oropharyngeal squamous cell carcinoma
Blue Earth Diagnostics Ireland Ltd
Treatment of human papilloma virus (HPV) associated infections and cancers
1 trial -
A phase 1, Pharmacokinetic Comparison of Vonafexor Acid and Its Lysine Salt (EYP651) and Evaluation of Potential Drug-Drug Interactions.
Lacuna Pharma Pty Ltd
Healthy volunteers, Impaired renal function and suspected MASH
1 trial -
A phase 1, randomised, double-blind, placebo-controlled, single ascending dose and multiple ascending dose study to evaluate the safety, tolerability, and pharmacokinetics in healthy adult subjects after subcutaneous injection of TISA-818-Inj-5mg/mL.
Lacuna Pharma Pty Ltd
Idiopathic pulmonary fibrosis
1 trial -
A phase I open-label, multi-center study to evaluate the safety, tolerability, dosimetry, and preliminary activity of [177Lu]Lu-DFC413 and safety and imaging properties of [68Ga]Ga-NNS309 in patients with solid tumors
Novartis Pharmaceuticals
Locally advanced unresectable or metastatic colorectal cancer (CRC), Locally advanced unresectable or metastatic pancreatic ductal adenocarcinoma (PDAC), Locally advanced unresectable or metastatic non-small cell lung cancer (NSCLC), Locally advanced unresectable or metastatic soft tissue sarcoma (excluding GIST and Kaposi sarcoma), Locally advanced unresectable or metastatic HR+/HER2- ductal or lobular breast cancer (BC), Locally advanced unresectable or metastatic triple negative breast cancer (TNBC)
1 trial -
A pilot, open label, single dose, randomized, four-period, four-sequence, four-treatment crossover, comparative bioavailability study of UDCA PMCS 500 mg formulation 1 film-coated tablets (test 1 formulation), and UDCA PMCS 500 mg formulation 2 film-coated tablets (test 2 formulation), and UDCA PMCS 500 mg formulation 3 film-coated tablets (test 3 formulation), and reference formulation in healthy, male and female volunteers under fasting conditions.
s.r.o.
UDCA causes a reduction in cholesterol saturation of the bile by inhibiting cholesterol absorption in the intestine and reducing cholesterol secretion into the bile. Presumably, cholesterol gallstones are gradually dissolved by dispersion of the cholesterol and formation of liquid crystals.
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