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ACTIVE NOT RECRUITING
NCT07090655
EARLY_PHASE1

A Phase 1 Study of Budoprutug (TNT119) Subcutaneous and Intravenous Injections in Normal Healthy Volunteers

Sponsor: Climb Bio, Inc.

View on ClinicalTrials.gov

Summary

The main objective is to assess the safety and tolerability of subcutaneous and intravenous injection forms of budoprutug in healthy volunteers.

Official title: A Phase 1, Randomized, Double-blind, Placebo-controlled, Single-ascending-dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneous and Intravenous Injections of Budoprutug (TNT119) in Normal Healthy Volunteers

Key Details

Gender

All

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

38

Start Date

2025-08-11

Completion Date

2026-06

Last Updated

2026-03-13

Healthy Volunteers

Yes

Interventions

DRUG

Budoprutug

Subcutaneous or IV administration

DRUG

Placebo

Placebo comparator

Locations (1)

Nucleus Network Brisbane

Brisbane, Australia