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Ovarian Cancer Real World Evidence study to evaluate the baseline demographics and clinicopathological characteristics of patients initiated on Olaparib.

An ambispective crosssectional multi-center non interventional cohort study to evaluate the clinical profile of ovarian cancer patients initiated on Olaparib and correlation of mutation status (BRCA & HRD) with clinicopathologic characteristics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/092561
Enrollment
250
Registered
2025-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: C569- Malignant neoplasm of unspecifiedovary

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

Cipla Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patient of more than or equal to 18 years of age Previously treated or newly diagnosed ovarian primary peritoneal or fallopian tube cancer patients prescribed on Olaparib na ve or initiated equal to or less than 3 months Mutation status BRCA positive or HRD plus BRCA negative or HRD positive

Exclusion criteria

Exclusion criteria: Failed to provide written informed consent Any medical condition that in the opinion of the investigator would interfere with safe completion of the study, or were participating in any other clinical

Design outcomes

Primary

MeasureTime frame
Baseline demography including molecular characteristics age gender comorbidities primary treatment family history BRCA1 BRCA2 mutation and HRD statusTimepoint: Baseline

Secondary

MeasureTime frame
Assess the co-relation of BRCA and HRD status Lifestyle medical history and symptoms Family history Histopathologic type of OC Previous lines of treatmentTimepoint: Baseline

Countries

India

Contacts

Public ContactDr Devang Sarvaiya

Cipla Limited

dr.sucheta@cipla.com9820305797

Outcome results

None listed

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