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OncoMatch/Clinical Trials/NCT07322094

CATALINA-4: A Study to Investigate the Safety and Efficacy of TORL-1-23 With Chemotherapy Given Before Initial Surgery in Women With Advanced Stage Ovarian Cancer

Is NCT07322094 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including TORL-1-23 and paclitaxel and TORL-1-23 and carboplatin for figo stage iii and iv ovarian cancer.

Phase 1/2RecruitingTORL Biotherapeutics, LLCNCT07322094Data as of Jun 2026

Treatment: TORL-1-23 and paclitaxel · TORL-1-23 and carboplatin · TORL-1-23, paclitaxel, and carboplatinA Phase 1B/2 Study to Investigate the Safety and Efficacy of TORL-1-23 with Chemotherapy Given Before Initial Surgery in Women with Advanced Stage Ovarian Cancer

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Extracted eligibility criteria

Treatments studied

Chemotherapy

TORL-1-23 and paclitaxelTORL-1-23 and carboplatinTORL-1-23, paclitaxel, and carboplatin

Cancer type

Ovarian Cancer

Biomarker criteria

Required: CLDN6 overexpression

Positive for claudin 6 (CLDN6) expression

Disease stage

Required: Stage III, IV

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 70
Female only

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy

Prior systemic treatment for the disease under study

Cannot have received: surgery

Prior surgery

Cannot have received: radiation therapy

Prior radiation therapy to the abdomen or pelvis

Cannot have received: chemotherapy

Exception: within 5-half-lives of C1D1

Current recipient or receipt within 5-half-lives of C1D1 of chemotherapy, biologic/targeted therapy, immunomodulator therapy for any disease indication

Cannot have received: biologic/targeted therapy

Exception: within 5-half-lives of C1D1

Current recipient or receipt within 5-half-lives of C1D1 of chemotherapy, biologic/targeted therapy, immunomodulator therapy for any disease indication

Cannot have received: immunomodulator therapy

Exception: within 5-half-lives of C1D1

Current recipient or receipt within 5-half-lives of C1D1 of chemotherapy, biologic/targeted therapy, immunomodulator therapy for any disease indication

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • UCLA · Los Angeles, California

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07322094 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require CLDN6?

Yes, CLDN6 overexpression is a required biomarker for enrollment.

What disease stage is eligible?

Stage III or IV is required.

Is there an age limit?

Yes. Patients must be 70 years or younger.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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