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Active Not RecruitingNCT06334432

Safety and Efficacy Study of NUV-1511 in Adult Patients With Advanced Solid Tumors

A Phase 1/2, First-in-Human, Safety and Efficacy Study of NUV-1511 in Adult Patients With Advanced Solid Tumors

Status
Active Not Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
466 (estimated)
Sponsor
Nuvation Bio Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

NUV-1511-01 is a first-in human, open- label, Phase 1/2 to evaluate the safety and efficacy of NUV-1511 in patients with advanced solid tumors. The Phase 1 portion include patients with advanced solid tumors and is designed to determine the safety and the tolerability of doses of NUV-1511. In Phase 2, NUV-1511 will be given to determine the efficacy of patients with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGNUV-1511Novel small molecule

Timeline

Start date
2024-03-14
Primary completion
2027-03-01
Completion
2027-10-01
First posted
2024-03-28
Last updated
2026-01-14

Locations

8 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06334432. Inclusion in this directory is not an endorsement.