Study of Lurbinectedin (PM01183) in Combination With Cisplatin in Patients With Solid Tumors

Sponsor

PharmaMar (Industry)

Overall Status

Completed

CT.gov ID

NCT01980667

Collaborator

(none)

Enrollment

Locations

Arm

29.2

Duration (Months)

13.7

Patients Per Site

0.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Clinical and Pharmacokinetic Study of Lurbinectedin (PM01183) in Combination with Cisplatin in Patients with Advanced Solid Tumors to determine the recommended dose (RD) of PM01183 in combination with cisplatin, to characterize the safety profile, the pharmacokinetics (PK) of this combination, to obtain preliminary information on the clinical antitumor activity and to conduct an exploratory pharmacogenomic (PGx) analysis.

Condition or Disease	Intervention/Treatment	Phase
Advanced Solid Tumors	Drug: lurbinectedin (PM01183) Drug: Cisplatin	Phase 1

Study Design

Study Type:

Interventional

Actual Enrollment :

41 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase I Multicenter, Open-label, Clinical and Pharmacokinetic Study of Lurbinectedin (PM01183) in Combination With Cisplatin in Patients With Advanced Solid Tumors

Study Start Date :

Jul 30, 2014

Actual Primary Completion Date :

Jan 5, 2017

Actual Study Completion Date :

Jan 5, 2017

Arms and Interventions

Arm	Intervention/Treatment
Experimental: lurbinectedin (PM01183) / cisplatin Patients will receive cisplatin as a 90-min i.v. infusion. In addition, patients will receive PM01183 as an i.v. infusion over 1-hour.	Drug: lurbinectedin (PM01183) lurbinectedin (PM01183) is presented as powder for concentrate for solution for infusion with two strengths, 1-mg and 4-mg vials. Drug: Cisplatin vials containing 1 mg/ml concentrate for solution for infusion

Arm

Intervention/Treatment

Experimental: lurbinectedin (PM01183) / cisplatin

Patients will receive cisplatin as a 90-min i.v. infusion. In addition, patients will receive PM01183 as an i.v. infusion over 1-hour.

Drug: lurbinectedin (PM01183)

lurbinectedin (PM01183) is presented as powder for concentrate for solution for infusion with two strengths, 1-mg and 4-mg vials.

Drug: Cisplatin

vials containing 1 mg/ml concentrate for solution for infusion

Outcome Measures

Primary Outcome Measures

Recommended dose (RD) of the combination PM01183 and cisplatin [30 months]
To determine the recommended dose (RD) of PM01183 in combination with cisplatin every three weeks (q3wk) with or without aprepitant in patients with advanced solid tumors. The RD will be the dose level (DL) immediately below the maximum tolerated dose (MTD), that is, the highest DL explored at which less than one third of evaluable patients experience a DLT during Cycle 1.

Secondary Outcome Measures

Pharmacokinetics (PK) characterisation of Cmax (maximum concentratio), AUC (area under the curve), CL (clearance), HL (half life) y Vss (volume of distribution) [30 months]
To characterize the pharmacokinetics (PK) parameters Cmax (maximum concentratio), AUC (area under the curve), CL (clearance), HL (half life) y Vss (volume of distribution ) of this combination in patients receiving/not receiving aprepitant and to explore factors that may affect individual variability in main PK parameters.
Pharmacogenomic (PGx) analysis [30 months]
To conduct an exploratory pharmacogenomic (PGx) analysis to identify and validate putative molecular markers associated with the clinical outcome of patients treated with PM01183 and cisplatin. These molecular markers would help in the future selection of patients who might preferentially benefit from PM01183 therapy, thus contributing to improve health care through a more individualized medicine.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Voluntarily signed written informed consent
Age ≥ 18 years old
Eastern Cooperative Oncology Group (ECOG) performance status (PS) of ≤ 1.
Life expectancy ≥ 3 months.
Patients with confirmed diagnosis of advanced solid tumors.
Patients may have received ≤ 2 chemotherapy-containing lines in the advanced setting.
Adequate bone marrow, renal, hepatic, and metabolic function (assessed ≤ seven days before inclusion in the study)
Recovery or stabilization to grade ≤ 1 from any adverse event derived from previous treatment (up to grade 2 alopecia or asthenia/fatigue are allowed).
No clinically significant changes in ECG.
At least four weeks since the last monoclonal antibody containing therapy or definitive radiotherapy (RT)
At least two weeks since the last biological/investigational single-agent therapy (excluding MAbs) and/or palliative RT (≤10 fractions or ≤30 Gy total dose)
Fertil women must have pregnancy excluded by appropriate testing before study entry

Exclusion Criteria:

Prior treatment with PM01183 or trabectedin.
Concomitant diseases/conditions:
History within the last year or presence of unstable angina, myocardial infarction, congestive heart failure, or clinically relevant valvular heart disease or symptomatic arrhythmia or any asymptomatic ventricular arrhythmia requiring ongoing treatment.
Ongoing, non-neoplastic, chronically active liver disease of any origin.
Active infection.
Patients who are requiring any ongoing oxygen support.
Known human immunodeficiency virus (HIV) infection.
Any other major illness.
Symptomatic or corticosteroid-requiring brain metastases or leptomeningeal disease involvement. Patients with asymptomatic documented stable brain metastases not requiring corticosteroids during the last three months are allowed.
Peripheral sensory/motor neuropathy grade >1. Hearing impairment grade >1.
Fertile men or women not using an effective method of contraception.
History of bone marrow or stem cell transplantation
Radiotherapye to >35% of the bone marrow.