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



Status:Completed
Conditions:Ovarian Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:10/20/2018
Start Date:May 2015
End Date:October 12, 2018

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

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).


Inclusion Criteria:

- Age >/= 18 years

- Confirmed diagnosis of unresectable epithelial ovarian, fallopian tube or primary
peritoneal cancer.

- Platinum-resistant disease (PFI: 1-6 months after last platinum-containing
chemotherapy).

- Evaluable disease according to Response Evaluation Criteria in Solid Tumors (RECIST)
v.1.1 criteria

- No more than three prior systemic chemotherapy regimens

- Eastern Cooperative Oncology Group (ECOG) performance status (PS) (ECOG PS) ≤ 2

- Adequate hematological, renal, metabolic and hepatic function

Exclusion Criteria:

- Concomitant diseases/conditions: cardiac disease, immunodeficiency, chronic active
hepatitis or cirrhosis, uncontrolled infection, bowel obstruction, any other major
illness

- Prior treatment with PM01183, trabectedin, or with both PLD and topotecan.

- Requirement of permanent or frequent (i.e., once per week) external drainages within
two weeks prior to randomization
We found this trial at
28
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Charlotte, North Carolina 28207
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Charlotte, North Carolina 28207
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Greenville, South Carolina 29605
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