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Poster Display

47P - Phase 1 Study to Assess the Safety and Efficacy of P-BCMA-ALLO1, a Fully Allogeneic CAR-T Therapy, in Patients with Relapsed / Refractory Multiple Myeloma (RRMM)

Date

08 Dec 2022

Session

Poster Display

Presenters

Mehmet Kocoglu

Citation

Annals of Oncology (2022) 16 (suppl_1): 100101-100101. 10.1016/iotech/iotech100101

Authors

M.H. Kocoglu1, A. Asch2, A. Ramakrishnan3, C. Bachier4, T. Martin5, T. Rodriguez6, K. McArthur7, C. Martin7, H. Namini7, E. Ostertag7, M. Spear7, E. Christie7, R. Belani7, M. Zhang7, S. Cranert7, J. Coronella7, D. Shedlock7, C. Costello8

Author affiliations

  • 1 University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore/US
  • 2 Stephenson Cancer Center, Oklahoma University Health Science Center, Oklahoma City/US
  • 3 Sarah Cannon Blood Cancer Center at St. David's South Austin, Austin/US
  • 4 Sarah Cannon Transplant and Cellular Therapy Program , Methodist Hospital, San Antonio/US
  • 5 UCSF Medical Center at Parnassus, San Francisco/US
  • 6 Advocate Lutheran General Hospital, Park Ridge/US
  • 7 Poseida Therapeutics, San Diego/US
  • 8 UCSD Moores Cancer Center, La Jolla/US

Resources

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Abstract 47P

Background

P-BCMA-ALLO1 is an allogeneic Chimeric Antigen Receptor T-cell (CAR-T) targeting B-cell Maturation Antigen (BCMA) being investigated in RRMM. P-BCMA-ALLO1 is manufactured using non-viral transposon-based integration (piggyBac®DNA Delivery System) that introduces a humanized anti-BCMA VH-based CAR producing a highly enriched T stem cell memory product. The Cas-CLOVER™ Site-Specific Gene Editing System eliminates endogenous T cell receptor (TCR) expression via knockout of the TCR beta chain 1 gene to prevent graft-vs-host disease, and the beta-2 microglobulin gene to reduce MHC class I expression to eliminate host-vs-graft responses. P-BCMA-ALLO1 demonstrated compelling activity in MM xenografts, providing rationale for this first-in-human phase I study.

Methods

The primary objective is to assess the safety and maximum tolerated dose based on dose limiting toxicity (DLT) in RRMM patients who have received a proteasome inhibitor, immunomodulatory drug and anti-CD38 monoclonal antibody. Secondary objectives will assess the anti-myeloma effect. The protocol utilizes standard 3+3 dose escalation to treat 40 patients. Patients receive lymphodepleting chemotherapy (LDC) with cyclophosphamide (300 mg/m2/day) / fludarabine (30 mg/m2/day) on days -5, -4 and -3 followed by a single dose of P-BCMA-ALLO1 on Day 0.

Results

As of 21SEP2022, 7 patients were treated with P-BCMA-ALLO1. Six patients received the cohort 1 dose of 0.75 X 106 CAR-T cells/kg and 1 patient received the cohort 2 dose of 2 X 106 cells/kg. To date, 4 cohort 1 patients have completed the DLT evaluation period and are evaluable for response. Most adverse events (AE) were grade 1 and 2. One patient had a serious AE of G3 febrile neutropenia. DLTs, cytokine release syndrome and neurotoxicity have not been observed. To date, 1 patient achieved very good partial response, 2 patients achieved partial response, and 1 patient had stable disease. Responses were seen starting at week 2, and overall response rate is 75%.

Conclusions

Early results demonstrate acceptable toxicity profile and promising efficacy for P-BCMA-ALLO1. Dose escalation is ongoing. Updated safety and efficacy results will be presented.

Clinical trial identification

NCT04960579.

Legal entity responsible for the study

Poseida Therapeutics.

Funding

Poseida Therapeutics.

Disclosure

M.H. Kocoglu: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics. A. Asch: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics; Financial Interests, Personal and Institutional, Research Grant: Gilead Sciences. A. Ramakrishnan: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics. C. Bachier: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics. T. Martin: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics; Financial Interests, Personal and Institutional, Research Grant: Sanofi, Amgen, Janssen, Seattle Genetics; Financial Interests, Personal, Advisory Role: GSK, Juno, Roche. T. Rodriguez: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics; Financial Interests, Personal, Speaker’s Bureau: Kite Pharma, Sanofi, Jazz Pharmaceuticals. K. McArthur, C. Martin, H. Namini, E. Ostertag: Financial Interests, Personal and Institutional, Full or part-time Employment: Poseida Therapeutics. M. Spear: Financial Interests, Personal, Stocks/Shares: Poseida Therapeutics; Financial Interests, Personal and Institutional, Full or part-time Employment: Denovo Biopharma. E. Christie: Financial Interests, Personal and Institutional, Full or part-time Employment: Poseida Therapeutics. R. Belani: Financial Interests, Personal and Institutional, Full or part-time Employment: Poseida Therapeutics; Financial Interests, Personal, Stocks/Shares: Amgen. M. Zhang: Financial Interests, Personal and Institutional, Full or part-time Employment: Poseida Therapeutics; Financial Interests, Personal, Stocks/Shares: BeiGene. S. Cranert, J. Coronella, D. Shedlock: Financial Interests, Personal and Institutional, Full or part-time Employment: Poseida Therapeutics. C. Costello: Financial Interests, Personal and Institutional, Principal Investigator: Poseida Therapeutics; Financial Interests, Personal and Institutional, Research Grant: BMS, Takeda, Janssen, Pfizer.

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