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Completed Phase 3 Interventional Results available

Clinical Trial of Lurbinectedin (PM01183) in Platinum Resistant Ovarian Cancer Patients

ClinicalTrials.gov ID: NCT02421588

Public ClinicalTrials.gov record NCT02421588. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 6:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase III Randomized Clinical Trial of Lurbinectedin (PM01183) Versus Pegylated Liposomal Doxorubicin or Topotecan in Patients With Platinum-resistant Ovarian Cancer (CORAIL Trial)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Multicenter, open-label, randomized, controlled phase III clinical trial to evaluate the activity and safety of PM01183 versus PLD or topotecan as control arm in patients with platinum-resistant ovarian cancer. PM01183 will be explored as single agent in the experimental arm (Arm A) versus PLD or topotecan in the control arm (Arm B).

Study identification

NCT ID
NCT02421588
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
PharmaMar
Industry
Enrollment
442 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2015 (Type not available)
Primary completion
Oct 12, 2018 (Actual)
Completion
Oct 12, 2018 (Actual)
Last update posted
Apr 3, 2020

2015 – 2018

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
26
Facility City State ZIP Site status
1112 Peoria Arizona — —
1102 Greenbrae California — —
1103 La Jolla California — —
1116 Los Angeles California — —
1120 Los Angeles California — —
1113 Palo Alto California — —
1111 San Francisco California — —
1122 Santa Maria California — —
1123 West Hills California — —
1109 Augusta Georgia — —
1104 Indianapolis Indiana — —
1110 Covington Louisiana — —
1124 Scarborough Maine — —
1121 Brick New Jersey — —
1127 Albany New York — —
1105 New York New York — —
1117 Asheville North Carolina — —
1101 Charlotte North Carolina — —
1125 Charlotte North Carolina — —
1108 Durham North Carolina — —
1107 Columbus Ohio — —
1118 Dayton Ohio — —
1119 Pittsburgh Pennsylvania — —
1115 Greenville South Carolina — —
1129 Nashville Tennessee — —
1131 Fort Worth Texas — —
1128 Houston Texas — —
1106 Charlottesville Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02421588, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 3, 2020 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02421588 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →