Gotistobart Long Term Extension (LTE) Study

NCT07659379 · Status: NOT_YET_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2026-06-23

No results posted yet for this study

Summary

This LTE study will examine the long-term overall survival and safety of gotistobart in patients with advanced solid tumors.

Conditions

  • Advanced Solid Tumor

Interventions

DRUG

Gotistobart

ONC-392 will be given following parent trial

Sponsors & Collaborators

  • OncoC4, Inc.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-01
Primary Completion
2036-07-01
Completion
2037-01-01
FDA Drug
Yes

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07659379 on ClinicalTrials.gov