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Spots Global Cancer Trial Database for Safety, Pharmacokinetics and Preliminary Anti-Tumor Activity of Intravenous TKM-080301 in Subjects With Advanced Hepatocellular Carcinoma

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Trial Identification

Brief Title: Safety, Pharmacokinetics and Preliminary Anti-Tumor Activity of Intravenous TKM-080301 in Subjects With Advanced Hepatocellular Carcinoma

Official Title: Open-Label, Multi-Center, Phase 1, Dose Escalation Study With Phase 2 Expansion Cohort to Determine the Safety, Pharmacokinetics and Preliminary Anti-Tumor Activity of Intravenous TKM-080301 in Subjects With Advanced Hepatocellular Carcinoma

Study ID: NCT02191878

Interventions

TKM-080301

Study Description

Brief Summary: This study is an open-label, multi-center, phase 1, dose escalation study with a phase 2 expansion cohort to determine the safety, pharmacokinetics and preliminary anti-tumor activity of intravenous TKM-080301 in subjects with advanced hepatocellular carcinoma (HCC). This study is being done to: * Test the safety and tolerability of TKM-080301 in subjects with advanced hepatocellular carcinoma * Find the highest dose of TKM-080301 that can be given without causing side effects, called the maximum tolerated dose (MTD). * Provide a preliminary assessment of anti-tumor activity of TKM-080301

Detailed Description: Study design: Open label, multi-center, 3 + 3 dose-escalation study with an expansion cohort at the maximum tolerated dose (MTD) to investigate safety, tolerability, PK, and preliminary anti-tumor activity of TKM 080301 in subjects with HCC. Sequential cohorts of 3 to 6 subjects will receive escalating doses of TKM 080301 according to a pre-specified dose escalation scheme. Assessment of dose-limiting toxicities (DLTs) will be made during Cycle 1 to determine the maximum tolerated dose (MTD). Once the MTD level is established, approximately 20 subjects will be enrolled in an expansion cohort to further confirm the safety and tolerability of TKM-080301 at the MTD. Study Population: A minimum of 9 and up to approximately 18 adult male or female subjects with histologically or cytologically confirmed metastatic or locally advanced inoperable HCC and a life expectancy of 3 months or more are planned in the dose escalation phase. Approximately 20 subjects are planned in the expansion cohort. Study Treatment: TKM-080301 will be administered by intravenous (IV) infusion, once weekly for 3 consecutive weeks followed by a 1 week rest period. This 28-day treatment period constitutes 1 cycle. Subjects who demonstrate clinical benefit without progression per RECIST 1.1 guidelines may receive treatment beyond 6 cycles if the Investigator considers it is in the best interest of the subject, and only with the approval of the Medical Monitor. Subjects would then continue TKM 080301 therapy until withdrawal of consent, disease progression or unacceptable toxicity occurs. Pharmacokinetics (PK) Subjects will undergo blood sample collection for PK analysis during cycles 1 and 2. Study Duration: Each treatment cycle will have duration of 28 days and each subject will typically receive up to 6 cycles of treatment. The total duration of the study is expected to be approximately 28 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Clinical Research Center, Tucson, Arizona, United States

University of California San Francisco, San Francisco, California, United States

Kansas City Research Institute, Kansas City, Missouri, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

Mary Crowley Cancer Research Centers, Dallas, Texas, United States

Princess Margaret Hospital, Toronto, Ontario, Canada

Queen Mary Hospital, Hong Kong, , China

Seoul National University Hospital, Seoul, Gyeonggi-do, Korea, Republic of

Samsung Medical Center, Seoul, Gyeonggi-do, Korea, Republic of

ASAN Medical Center, Seoul, Gyeonggi-do, Korea, Republic of

Severence Hospital, Yonsei, University Health System, Seoul, , Korea, Republic of

National University Hospital, Singapore, , Singapore

National Taiwan University Hospital, Taipei, , Taiwan

Taipei Medical University Hospital, Shuang-Ho Hospital, Taipei, , Taiwan

Taipei Veterans General Hospital, Taipei, , Taiwan

Contact Details

Name: Mark Kowalski, M.D., Ph.D.

Affiliation: Tekmira Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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