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Recruiting Phase 1 Interventional

DBC-664 in Adult Patients With Solid Tumors

ClinicalTrials.gov ID: NCT07705035

Public ClinicalTrials.gov record NCT07705035. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1a/1b Open Label, Multicenter, Dose Escalation and Dose Expansion Study of the Safety, Pharmacokinetics, Pharmacodynamics, and Activity of DBC-664 in Adult Patients With Locally Advanced or Metastatic Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

DBC-664-ONC-101 is a first-in-human Phase 1a/1b open-label, multicenter study to evaluate the safety, tolerability, PK, pharmacodynamic, and preliminary anti-tumor activity of DBC-664 in patients with endometrial cancer, ovarian cancer, and other advanced solid tumors . This study is divided into 2 parts: Phase-1a Dose Escalation (Part 1), and Phase-1b Dose Expansion (Part 2). In each part, patients who meet specific eligibility criteria will be enrolled.

Study identification

NCT ID
NCT07705035
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Duboce Biopharmaceuticals, Inc.
Industry
Enrollment
210 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2026 (Actual)
Primary completion
Apr 1, 2030 (Estimated)
Completion
Apr 1, 2030 (Estimated)
Last update posted
Sep 29, 2026

2026 – 2030

United States locations

U.S. sites
6
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
Sarah Cannon Research Institute - Denver HealthONE Denver Colorado 80218 Recruiting
START Midwest Grand Rapids Michigan 49546 Recruiting
START New Jersey East Brunswick New Jersey 08816 Recruiting
START New York Lake Success New York 11402 Recruiting
SCRI Oncology Partners Nashville Tennessee 37203 Recruiting
START San Antonio San Antonio Texas 78229 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07705035, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 29, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07705035 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →