Safety and Efficacy of ALLO-605 an Anti-BCMA Allogeneic CAR T Cell Therapy in Patients With Relapsed/Refractory Multiple Myeloma
Launched by ALLOGENE THERAPEUTICS · Aug 4, 2021
Trial Information
Current as of July 21, 2025
Terminated
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Documented diagnosis of relapsed/refractory multiple myeloma (MM)
- • Subjects must have measurable disease
- • Subjects must have received ≥3 prior MM lines of therapy
- • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- • Adequate hematologic, renal, liver, pulmonary, and cardiac functions
- • Life expectancy of at least 3 months without treatment
- Exclusion Criteria:
- • Subjects with known active or history of central nervous system (CNS) or leptomeningeal involvement of myeloma or plasma cell leukemia
- • Current or history of thyroid disorder (including hyperthyroidism), except for subjects with hypothyroidism controlled on a stable dose of hormone replacement therapy
- • Autologous stem cell transplantation within last 6 weeks prior to the start of lymphodepletion
- • Any prior allogeneic hematopoietic stem cell transplantation
- • Systemic anti-cancer therapy within 2 weeks prior to the start of lymphodepletion
About Allogene Therapeutics
Allogene Therapeutics is a pioneering biotechnology company focused on developing groundbreaking allogeneic cell therapies for the treatment of cancer. Leveraging advanced gene-editing technologies, Allogene strives to create innovative, off-the-shelf CAR T-cell therapies that are designed to enhance patient accessibility and improve treatment outcomes. With a commitment to scientific excellence and a robust pipeline of clinical programs, Allogene Therapeutics aims to transform the landscape of cancer treatment, providing hope and new possibilities for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Houston, Texas, United States
San Antonio, Texas, United States
Austin, Texas, United States
Denver, Colorado, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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