A Multicenter Phase I Clinical Study of a New Compound P1446A-05 in Patients With Advanced Refractory Malignancies
- Conditions
- Cancer
- Interventions
- Drug: P1446A-05
- Registration Number
- NCT00772876
- Lead Sponsor
- Piramal Enterprises Limited
- Brief Summary
This is a phase I study of a novel compound P1446A-05. Aim of this study is to identify the the recommended phase II dose of the drug and to determine the nature of adverse effects associated with the drug. P1446A-05 capsules will be given continuously (28 days in each 28 day cycle) to patients suffering from advanced malignancies with no effective treatment available. The dose of the study agent will be lower i.e. 75 mg per day for initial patients. If this dose is found safe, higher dose will be administered to next set of (three to six) patients. This will continued till the safest and best dose is identified. Treatment will be given for 4 cycles and continued further if found effective. Dose schedule may be modified to introduce treatment holiday,if frequent adverse effects are seen on continuous administration.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 39
- Histologically and/ or cytologically confirmed solid malignant tumor or Malignant Lymphoma (excluding CNS Lymphoma and multiple myeloma) that is refractory to currently available treatment or for which no standard treatment exists
- Measurable disease
- Must have completed any prior chemotherapy, radiotherapy, biologic/targeted anti-cancer therapy or surgery at least 4 weeks (at least 6 weeks for nitrosureas and mitomycin C; 3 months for monoclonal antibodies, radioactive monoclonal antibodies or any radio- or toxin- immunoconjugates) before study entry and subjects must have recovered (to ≤grade 1) from the toxic effects from any prior therapy.
- Must not have had more than 40% of their bone marrow radiated and must have either measurable disease outside the field or progression post radiation therapy.
- Age ≥ 18 years
- ECOG performance status ≤ 2
- Life expectancy of at least 12 weeks
- Normal organ and marrow function as defined below:
Hemoglobin >/= 90 g/L Leukocytes >/=3 x 109/L Absolute Neutrophil Count (ANC) >/=1.5 x 109/L Platelets >/=100 x 109/L Total bilirubin </= 1.5 X institutional Upper Limit of Normal (ULN) AST(SGOT) </=2.5 X institutional ULN ALT(SGPT) </=2.5 X institutional ULN Creatinine </=1.5 X institutional ULN
- Ability to understand and willingness to sign a written informed consent document.
- autologous or allogeneic bone marrow transplant within 6 months of day 1 of study drug administration
- Known brain metastases at the time of screening
- Any other investigational drug within 1 month prior to day 1 of study drug administration or not recovered (to ≤grade 1) from adverse effects of the investigational agent received prior to this period.
- History of allergic reactions attributed to compounds of similar chemical structure to P1446A-05.
- On immunosuppressive therapy.
- History of unstable angina or myocardial infarction or stroke within 6 months prior to Day 1 of study drug administration.
- Uncontrolled inter-current illness including, but not limited to active infection, symptomatic congestive heart failure, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Known to be suffering from infection with HIV, Tuberculosis, Hepatitis C or Hepatitis B.
- Pregnant or lactating women
- Women of childbearing potential [defined as a sexually mature woman who has not undergone hysterectomy or who has not been naturally postmenopausal for at least 24 consecutive months (i.e. who has had menses any time in the preceding 24 consecutive months)] and men, not agreeing to use adequate contraception (two methods of contraception, including at least one barrier method, - i.e. : hormonal and a barrier method of birth control or abstinence) prior to study entry (after signing the informed consent document), during the duration of study participation and for at least 4 weeks after withdrawal from the study drug, unless they are surgically sterilised.
- Any condition, including laboratory abnormalities, that in the opinion of the investigator places the subject at an unacceptable risk or deems the subject not suitable for participation in the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description P1446A-05 P1446A-05 Single arm of the study drug. This being a dose escalation study, patient will receive a dose depending on the stage of the trial.
- Primary Outcome Measures
Name Time Method Number of Dose Limiting Toxicities at a dose level Cycle 1 of each subject
- Secondary Outcome Measures
Name Time Method Response rate At the end of every 2 cycles
Trial Locations
- Locations (4)
Tom Baker Cancer Centre
🇨🇦Calgary, Alberta, Canada
London Health Sciences Centre (LHSC)
🇨🇦London, Ontario, Canada
British Columbia Cancer Agency (BCCA),
🇨🇦Vancouver,, British Columbia, Canada
Cross Cancer Institute (CCI),
🇨🇦Edmonton,, Alberta, Canada