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RECRUITING Phase 1

A Study of CUSP06 in Patients With Platinum-Refractory/Resistant Ovarian Cancer and Other Advanced Solid Tumors

NCT06234423 · View on ClinicalTrials.gov ↗

Study Summary

This phase 1 study will evaluate the safety, tolerability, pharmacokinetics, and efficacy of CUSP06 in patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors.

Interventions

  • DRUG CUSP06

Study Locations (15)

Texas

  • MD Anderson Cancer Center — Houston
  • NEXT Oncology — Houston
  • START San Antonio — San Antonio

Florida

  • Mount Sinai Medical Center — Miami Beach
  • Florida Cancer Specialists — Sarasota

New York

  • NYU Cancer Institute Clinical Cancer Center — New York
  • Memorial Sloan Kettering Cancer Center — New York

Colorado

  • Sarah Cannon Research Institute at HealthONE — Denver

Connecticut

  • Yale University — New Haven

Massachusetts

  • Dana Farber Cancer Institute — Boston

Michigan

  • START Midwest — Grand Rapids

Oklahoma

  • Stephenson Cancer Center — Oklahoma City

Trial Details

FieldValue
Enrollment Target 263 participants
Start Date 2024-02-09
Est. Completion 2027-10-31
Phase Phase 1

Sponsor

OnCusp Therapeutics

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06234423

The ClinicalTrials.gov registry entry for NCT06234423 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 263 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is OnCusp Therapeutics, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 1 intervention — of which CUSP06 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06234423 reports 15 study locations spanning 11 distinct geographic areas — top geographies include Texas, Florida, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06234423 about?

NCT06234423 is a clinical study titled "A Study of CUSP06 in Patients With Platinum-Refractory/Resistant Ovarian Cancer and Other Advanced Solid Tumors". This phase 1 study will evaluate the safety, tolerability, pharmacokinetics, and efficacy of CUSP06 in patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors.

What is the current status of trial NCT06234423?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 263 participants. The study started on 2024-02-09. Estimated completion is 2027-10-31.

What conditions does trial NCT06234423 study?

This clinical trial studies the following conditions: Ovarian Cancer, Solid Tumor. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06234423?

The interventions under investigation include: CUSP06 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06234423?

This trial is sponsored by OnCusp Therapeutics, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06234423 being conducted?

This trial has 15 study locations across Colorado, Connecticut, Florida, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial