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A prospective, single-arm clinical study of platinum plus pemetrexed combined with anlotinib in the treatment of platinum-resistant and relapsed ovarian cancer

A prospective, single-arm clinical study of platinum plus pemetrexed combined with anlotinib in the treatment of platinum-resistant and relapsed ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104000
Enrollment
Unknown
Registered
2025-06-10
Start date
2025-06-15
Completion date
Unknown
Last updated
2025-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian cancer

Interventions

Experimental group:The patients were treated with platinum drugs and cytotoxic drugs pemetrexed combined with anlotinib

Sponsors

The First Hospital Affiliated to Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Females aged 18-70 years with platinum-resistant (defined as PFI =3.0*10^9/L, neutrophil count>=1.5*10^9/L, platelet count>=100*10^9/L, hemoglobin concentration>=90g/L. 9. Liver function: AST and ALT=60ml/min.

Exclusion criteria

Exclusion criteria: 1.The presence of symptoms and signs of active central nervous system metastasis. 2.Patients with >=4 recurrences. 3.Patients with allergy to platinum-based chemotherapy agents. 4.Allergy to pemetrexed, anlotinib and their excipients. 5.Accompanied by diseases that endanger the safety of the subjects or affect the completion of the study, including poorly controlled hypertension, poorly controlled diabetes, chronic obstructive pulmonary disease, pulmonary embolism, cerebral thrombosis or cerebral hemorrhage within half a year, myocardial infarction, severe congestive heart failure, etc. 6.Patients judged by the investigator to be ineligible for the study.

Design outcomes

Primary

MeasureTime frame
CR or PR;

Secondary

MeasureTime frame
Kelim score;Disease control rate;Duration of response;Progression-free survival;

Countries

China

Contacts

Public ContactLi Deng

The First Hospital Affiliated to Army Medical University

denglitmmu@163.com+86 18602383009

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026