Status:
COMPLETED
Safety Study to Evaluate CHR-2797 in Patients With Advanced Tumours
Lead Sponsor:
Chroma Therapeutics
Collaborating Sponsors:
Institute of Cancer Research, United Kingdom
Conditions:
Advanced Solid Tumors
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The primary objective of this study was to determine the safety, tolerability, dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) of CHR-2797 when administered orally, once daily, to patien...
Eligibility Criteria
Inclusion
- Signed, informed consent
- Histological or cytologically confirmed malignant solid tumour refractory to standard therapy or for which no standard therapy exists
- Evaluable disease
- Recovered from the acute adverse effects of prior therapies (excluding alopecia and grade 1 neuropathy)
- Adequate bone marrow, hepatic and renal function including the following:
- Hb ≥ 9.0 g/dl, absolute neutrophil count ≥ 1.5 x 109/L, platelets ≥ 100x109/L
- Total bilirubin ≤ 1.5 x upper normal limit
- AST and ALT ≤ 2.5 x upper normal limit (or ≤ 5 x UNL in the presence of liver metastases)
- Creatinine ≤1.5 x upper normal limit
- Age \< 18 years
- Performance status (PS) \< 2 (ECOG scale)
- Estimated life expectancy greater than 3 months
- Female patients with reproductive potential had to have a negative serum pregnancy test within 7 days of treatment. Both women and men had to agree to use a medically acceptable method of contraception throughout the treatment period and for 3 months after discontinuation of treatment. Acceptable methods of contraception included IUD, oral contraceptive, sub-dermal implant and double barrier (condom with a contraceptive sponge or contraceptive pessary)
Exclusion
- Anti-cancer therapy including chemotherapy, radiotherapy, endocrine therapy, immunotherapy or use of other investigational agents within the 4 weeks prior to study entry (or a longer period depending on the defined characteristics of the agents used e.g. 6 weeks for mitomycin or nitrosourea). In patients with progressive disease (PD), continuation of LHRH agonists for prostate cancer, bisphosphonates for bone disease and corticosteroids was permitted provided the dose was stable before and during the study
- Co-existing active infection or serious concurrent illness
- Significant cardiovascular disease as defined by
- History of congestive heart failure requiring therapy
- History of unstable angina pectoris or myocardial infarction up to 6 months prior to study entry
- Presence of severe valvular heart disease
- Presence of a ventricular arrhythmia requiring treatment
- Any co-existing medical condition that in the Investigator's judgement substantially increased the risk associated with the patient's participation in the study
- Psychiatric disorders or altered mental status precluding understanding of the informed consent process and/or completion of the necessary studies
- Gastrointestinal disorders that might have interfered with absorption of the study drug
- Persistent grade 2 or greater toxicities from any cause
- Patients with known brain tumours or metastases should have been excluded from this clinical study because of their poor prognosis and because they often develop progressive neurologic dysfunction that would have confounded the evaluation of neurologic and other AEs
- Pregnant or breast-feeding women
Key Trial Info
Start Date :
October 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2008
Estimated Enrollment :
41 Patients enrolled
Trial Details
Trial ID
NCT00692354
Start Date
October 1 2004
End Date
March 1 2008
Last Update
August 6 2010
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