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Study identifier: NCT07500181 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BAL2420 in Healthy Adult Subjects

Condition: Healthy  ·  Sponsor: Basilea Pharmaceutica

PhasePhase 1
Planned participants136
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

BAL2420 (also known as BAL0302420) is being developed as an antibacterial agent for the treatment of severe infections caused by Gram-negative bacteria. In this study, the sponsor aims to investigate the safety, tolerability and pharmacokinetics (PK) of BAL2420 following administration of single ascending doses (Part A) and multiple ascending doses (Parts B and C) in healthy adult volunteers. In all parts of the study, in each cohort, a different dose of study drug is to be investigated against a matched placebo in a randomized and double-blind manner.

This description comes directly from the study's public registry record.

Talk to the study team

Thomas Kaindl, MD  ·  +41615671505  ·  thomas.kaindl@basilea.com

Always discuss trial participation with your own doctor first.

Locations (1)

ICON Early Clinical & Bioanalytical SolutionsGroningen, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT07500181