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Spots Global Cancer Trial Database for Glucarpidase After High-Dose Methotrexate in Patients With Osteosarcoma

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Trial Identification

Brief Title: Glucarpidase After High-Dose Methotrexate in Patients With Osteosarcoma

Official Title: An Open-Label, Multi-Institutional Pilot Study to Assess the Use of Glucarpidase in Adult Patients With Osteosarcoma Receiving High-Dose Methotrexate

Study ID: NCT03960177

Conditions

Osteosarcoma

Study Description

Brief Summary: This early phase I trial studies how well glucarpidase works in reducing toxicity in patients with osteosarcoma receiving high dose methotrexate treatment. Glucarpidase may reduce the levels of methotrexate in patients' blood and lead to shorter hospitalizations and a reduction in toxicities.

Detailed Description: PRIMARY OBJECTIVE: I. To determine the rate of completion of 4 planned high dose methotrexate (HDMTX) doses when glucarpidase is administered after each dose. SECONDARY OBJECTIVES: I. To assess the length of hospital stay (LOS) associated with methotrexate (MTX) clearance following administration of glucarpidase 24 hours after HDMTX. II. To assess the LOS associated with all causes following administration of glucarpidase 24 hours after HDMTX. III. To assess the impact of glucarpidase administration on HDMTX efficacy. IV. To assess the safety and tolerability of 4 doses of HDMTX administered with glucarpidase in an adult osteosarcoma population. V. To assess the efficacy of glucarpidase flat dose of 1,000 units. OUTLINE: Patients receive standard of care HDMTX intravenously (IV) over 4 hours on day 1 of weeks 4, 5, 9, and 10. After 24 and 48 hours after the start of each HDMTX infusion, patients also receive glucarpidase IV over 5 minutes in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 32 weeks.

Keywords

Eligibility

Minimum Age: 25 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic in Florida, Jacksonville, Florida, United States

Mayo Clinic in Rochester, Rochester, Minnesota, United States

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

OHSU Knight Cancer Institute, Portland, Oregon, United States

University of Pennsylvania/Abramson Cancer Center, Philadelphia, Pennsylvania, United States

Contact Details

Name: Lara E Davis

Affiliation: OHSU Knight Cancer Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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