Basilea Pharmaceutica

21 total trials 3 currently recruiting 14 completed

Basilea Pharmaceutica sponsors 21 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 14 completed. 5 of these trials are in Phase 3-4 (later-stage) and 16 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Pharmacokinetics, with 2 trials.

Trial Pipeline

21 total, page 1 of 1

RECRUITING Phase 3

A Phase 3 Efficacy and Safety Study of Fosmanogepix for the Treatment of Adult Patients With Invasive Mold Infections.

NCT06925321

RECRUITING Phase 1

Safety and PK of Ceftibuten-ledaborbactam Etzadroxil Fixed-dose Combination

NCT06733675

RECRUITING Phase 3

A Phase 3 Efficacy and Safety Study of Fosmanogepix for the Treatment of Adult Participants With Candidemia and/or Invasive Candidiasis.

NCT05421858

COMPLETED Phase 1

Plasma and Intrapulmonary Pharmacokinetics of Ceftibuten and Ledaborbactam in Healthy Male and Female Participants 18 to ≤55 Years of Age

NCT06665555

COMPLETED Phase 3

Late-onset Sepsis in Term and Pre-term Neonates and Infants up to 3 Months of Age

NCT05856227

COMPLETED Phase 1

A Clinical Trial of the Study Medicine (Called Fosmanogepix) in Participants With Varying Degrees of Hepatic Function.

NCT05582187

COMPLETED Phase 1

Ceftibuten/VNRX-7145 in Participants With Varying Degrees of Renal Function

NCT05488678

COMPLETED Phase 1

Food Effect on Ceftibuten/VNRX-7145 in Healthy Participants

NCT05527834

COMPLETED Phase 1

A Bioequivalence Study of APX001 High-load and Low-load Tablets

NCT05491733

TERMINATED Phase 1

Derazantinib Alone or in Combination With Paclitaxel, Ramucirumab or Atezolizumab in Gastric Adenocarcinoma

NCT04604132

COMPLETED Phase 1

VNRX-7145 SAD/MAD Safety and PK in Healthy Adult Volunteers

NCT04243863

TERMINATED Phase 2

Open-label Study of APX001 for Treatment of Patients With Invasive Mold Infections Caused by Aspergillus or Rare Molds

NCT04240886

COMPLETED Phase 1

Derazantinib and Atezolizumab in Patients With Urothelial Cancer

NCT04045613

COMPLETED Phase 2

An Efficacy and Safety Study of APX001 in Non-Neutropenic Patients With Candidemia

NCT03604705

COMPLETED Phase 3

Ceftobiprole in the Treatment of Patients With Staphylococcus Aureus Bacteremia

NCT03138733

COMPLETED Phase 3

Ceftobiprole in the Treatment of Patients With Acute Bacterial Skin and Skin Structure Infections

NCT03137173

TERMINATED Phase 1

Microtubule-Targeted Agent BAL101553 and Radiation Therapy in Treating Patients With Newly Diagnosed Glioblastoma

NCT03250299

COMPLETED Phase 2

Derazantinib in Subjects With FGFR2 Gene Fusion-, Mutation- or Amplification- Positive Inoperable or Advanced Intrahepatic Cholangiocarcinoma

NCT03230318

TERMINATED Phase 1

Pharmacokinetics and Safety of Ceftobiprole in Neonates and Infants up to 3 Months Treated With Systemic Antibiotics

NCT02527681

COMPLETED Phase 1

Phase 1/2 Study of Derazantinib (ARQ 087) in Adult Subjects With Advanced Solid Tumors With FGFR Genetic Alterations

NCT01752920

COMPLETED Phase 1

Open Label Study of Ceftobiprole to Evaluate Pharmacokinetics in Adults Hospitalized in the ICU

NCT00770978

What the Pipeline for Basilea Pharmaceutica Shows

According to the ClinicalTrials.gov registry, Basilea Pharmaceutica is linked to 21 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 14% of the sponsor's indexed portfolio, and 14 are already marked complete, representing roughly 67% of the total.

The phase mix for Basilea Pharmaceutica reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 16 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Basilea Pharmaceutica is Pharmacokinetics with 2 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.