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Clinical Trials/NCT07454018
NCT07454018
Not yet recruiting
Phase 2

A Single-Arm, Exploratory, Multicenter Study Evaluating Iparomlimab/Tuvonralimab Combined With Standard Chemotherapy Followed by Olaparib in Platinum-Sensitive Recurrent Ovarian Cancer

The First Affiliated Hospital of Soochow University0 sites45 target enrollmentStarted: March 1, 2026Last updated:

Overview

Phase
Phase 2
Status
Not yet recruiting
Sponsor
The First Affiliated Hospital of Soochow University
Enrollment
45
Primary Endpoint
Progression-Free Survival (PFS)

Overview

Brief Summary

This is a prospective, open-label, single-arm, multicenter exploratory clinical study designed to evaluate the efficacy and safety of iparomlimab/tuvonralimab (QL1706), a bispecific antibody targeting programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), in combination with standard platinum-based chemotherapy followed by olaparib in patients with platinum-sensitive recurrent epithelial ovarian cancer.

Eligible participants are women aged 18-75 years with histologically or cytologically confirmed non-mucinous epithelial ovarian cancer (including serous carcinoma, clear cell carcinoma, endometrioid carcinoma, and carcinosarcoma) who experience first or second recurrence at least 6 months after the last platinum-containing chemotherapy, have measurable disease per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1), an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-1, and are deemed not suitable for surgery by the investigator.

The study consists of a screening period (up to 28 days), a treatment period, and a follow-up period. Treatment is administered in 3-week cycles and continues until disease progression, unacceptable toxicity, withdrawal of consent, loss of clinical benefit per investigator judgment, completion of 2 years of iparomlimab/tuvonralimab (QL1706), or other protocol-defined reasons. Safety assessments are performed regularly during treatment; a safety follow-up visit is conducted 30 (±7) days after the last dose, and survival follow-up is performed every 2 months thereafter. The primary objective is to explore the antitumor efficacy of the regimen in platinum-sensitive recurrent epithelial ovarian cancer, and the secondary objective is to characterize the safety profile of the combination strategy.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Female participants aged 18 to 75 years. Voluntarily provide written informed consent and able to comply with protocol requirements.
  • Histologically and/or cytologically confirmed recurrent non-mucinous epithelial ovarian cancer (including serous carcinoma, clear cell carcinoma, endometrioid carcinoma, and carcinosarcoma).
  • First or second recurrence after standard platinum-containing chemotherapy, with recurrence diagnosed ≥ 6 months after the last dose of platinum-containing chemotherapy (platinum-sensitive recurrence).
  • Not suitable for surgery as assessed by the investigator.
  • At least one measurable lesion per RECIST v1.
  • ECOG performance status 0-
  • If no prior BRCA1/2 mutation test result is available, willing to provide tumor tissue and/or peripheral blood for confirmation of BRCA status (archival or fresh tumor tissue preferred; if re-biopsy poses safety risk, may be discussed with medical monitor).
  • Prior exposure to PARP inhibitor(s) other than olaparib is allowed only if the prior PARPi exposure after first-line therapy was \>18 months for BRCA-mutated participants or \>12 months for BRCA wild-type participants, and recurrence occurred ≥12 months after the last PARPi dose.
  • Estimated life expectancy ≥ 3 months.
  • Adequate organ function: ANC ≥1.5×10\^9/L; platelets ≥100×10\^9/L; hemoglobin ≥90 g/L; serum albumin ≥30 g/L; TSH ≤1×ULN (if abnormal, FT3/FT4 within normal range); total bilirubin ≤1.5×ULN; AST/ALT ≤2.5×ULN (≤5×ULN if liver metastases); ALP ≤2.5×ULN; serum creatinine ≤1.5×ULN; INR ≤1.5 (if not on anticoagulation).

Exclusion Criteria

  • Any active autoimmune disease or history of autoimmune disease.
  • Mucinous ovarian cancer, sex cord-stromal tumors, or other non-eligible histologic types.
  • Uncontrolled pleural effusion, pericardial effusion, or ascites that cannot be stabilized despite repeated drainage or other interventions per investigator judgment.
  • Other active malignancy within 2 years prior to first dose.
  • Central nervous system metastases or carcinomatous meningitis.
  • Palliative radiotherapy or immunomodulatory agents (e.g., thymosin, interferon, IL-2) or antitumor Chinese patent medicines within 2 weeks prior to first dose; hormonal therapy within 1 week prior to first dose.
  • Use of immunosuppressive agents or systemic corticosteroids for immunosuppression (prednisone \>10 mg/day or equivalent) within 2 weeks prior to enrollment.
  • Prior immuno-oncology therapies targeting tumor immunity (e.g., PD-1/PD-L1/CTLA-4 inhibitors, immune checkpoint agonists such as ICOS/CD40/CD137/GITR/OX40 antibodies, or immune cell therapy).
  • Prior treatment with olaparib.
  • Concomitant use of strong/moderate CYP3A inhibitors (washout 2 weeks) or strong/moderate CYP3A inducers (washout 5 weeks for enzalutamide/phenobarbital; 3 weeks for others).

Arms & Interventions

Iparomlimab/Tuvonralimab + Carboplatin + Nab-paclitaxel → Olaparib

Experimental

Participants receive iparomlimab/tuvonralimab in combination with carboplatin and nab-paclitaxel administered in 3-week cycles during the induction phase. After completion of induction therapy, participants receive oral olaparib as maintenance therapy according to the study protocol until disease progression, unacceptable toxicity, withdrawal of consent, completion of 2 years of iparomlimab/tuvonralimab treatment, or other protocol-defined discontinuation criteria.

Intervention: Iparomlimab/Tuvonralimab (Drug)

Outcomes

Primary Outcomes

Progression-Free Survival (PFS)

Time Frame: Up to 24 months

Time from first dose to first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
The First Affiliated Hospital of Soochow University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jinhua Zhou

Director, Department of Obstetrics and Gynecology

The First Affiliated Hospital of Soochow University

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