Advanced Malignant Solid Tumors
Conditions
Keywords
PM2734, Tumors, PharmaMar, Erlotinib, Tarceva
Brief summary
Phase I multicenter, open-label, dose-escalating clinical and pharmacokinetic trial of PM02734 administered in combination with erlotinib to determine the safety and tolerability and to identify the dose limiting toxicity (DLT) and the recommended dose (RD) of the combination of PM02734 and erlotinib, in patients with advanced malignant solid tumors.
Detailed description
Phase I multicenter, open-label, dose-escalating clinical and pharmacokinetic trial of PM02734 administered in combination with erlotinib to determine the safety and tolerability and to identify the dose limiting toxicity (DLT) and the recommended dose (RD) of the combination of PM02734 and erlotinib, determine the preliminary pharmacokinetics (PK) of the combination, evaluate the preliminary PK/pharmacodynamic correlation, evaluate the preliminary antitumor activity, perform a preliminary pharmacogenomic (PGx) study to explore molecular predictors of response to ErbB receptor antagonists and PM02734 in patient with advanced malignant solid tumors.
Interventions
DRUGPM02734 and erlotinib
PM02734 drug product (DP) 1 mg/vial is a powder for concentrate for solution for infusion
DRUGErlotinib
Erlotinib is provided as 25 mg, 100 mg and 150 mg white film-coated tablets
Sponsors
PharmaMar
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Voluntary written informed consent form. * Histologically or cytologically confirmed advanced malignant solid tumors. * Measurable or non-measurable disease following (RECIST) * Age ≥ 18 years. * Life expectancy ≥ 3 months. * Performance status ECOG ≤ 2. * Recovery from any drug-related adverse events (AEs) derived from previous treatments. * Appropriate bone marrow, liver and renal function. * Left ventricular ejection fraction (LVEF) within normal limits for the institution. * Women of childbearing potential must have a negative serum pregnancy test before study entry. Both men and women must agree to use a medically acceptable method of contraception throughout the treatment period and for three months after discontinuation of treatment.
Exclusion criteria
* Prior therapy with PM02734. * Pregnant or lactating women. * Less than four weeks from radiation therapy. * Evidence of progressive central nervous system (CNS) metastases. or any symptomatic brain or leptomeningeal metastases. * Other relevant diseases or adverse clinical conditions. * Any other major illness that, in the Investigator's judgment. * Limitation of the patient's ability to comply with the treatment or to follow-up at a participating protocol. * Ingestion of potent cytochrome CYP3A4 inhibitors. * Treatment with any investigational product in the 30-day period prior to the first infusion. * Known hypersensitivity to any component of PM02734 or erlotinib.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the safety and tolerability and to identify the dose limiting toxicity (DLT) and the recommended dose (RD) of the combination of PM02734 and erlotinib | 2 years |
Secondary
| Measure | Time frame |
|---|---|
| To determine preliminary: pharmacokinetics (PK) , PK / pharmacodynamic correlation, antitumor activity, pharmacogenomic (PGx) study to explore molecular predictors of response. | 2 years |
Countries
Spain, United States
Outcome results
None listed