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Active Not RecruitingNCT05718557

Study of PYX-106 in Solid Tumors

A First-in-Human, Open-label, Multicenter, Phase 1 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of PYX-106 in Subjects With Advanced Solid Tumors

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
47 (actual)
Sponsor
Pyxis Oncology, Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to determine the recommended dose(s) of PYX-106 in participants with relapsed/refractory solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGPYX-106Intravenous (IV) infusion

Timeline

Start date
2023-05-23
Primary completion
2026-05-01
Completion
2026-05-01
First posted
2023-02-08
Last updated
2025-08-03

Locations

20 sites across 3 countries: United States, Belgium, Spain

Regulatory

Source: ClinicalTrials.gov record NCT05718557. Inclusion in this directory is not an endorsement.

Study of PYX-106 in Solid Tumors (NCT05718557) · Clinical Trials Directory