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PHE885 CAR-T therapy in adult participants with relapsed and refractory multiple myeloma

A Phase 2 study of PHE885, B-cell maturation Antigen (BCMA)-directed CAR-T Cells in adult participants with relapsed and refractory multiple myeloma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2013220012
Enrollment
13
Registered
2022-07-25
Start date
2022-08-15
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple myeloma

Interventions

Single infusion of PHE885

Sponsors

Yamauchi Kyosuke
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. >=18 years of age at the time of informed consent form (ICF) signature 2. Adult patients with relapsed and refractory multiple myeloma who have received at least 3 prior lines of therapy including an IMiD (e.g., lenalidomide or pomalidomide), a proteasome inhibitor (e.g., bortezomib, carfilzomib), and an approved anti-CD38 antibody (e.g., daratumumab, isatuximab), and have documented evidence of disease progression (IMWG criteria) 3. Must be refractory to the last treatment regimen (defined as progressive disease on or within 60 days measured from last dose of last regimen). 4. Measurable disease at enrollment as defined by the protocol 5. Eastern Cooperative Oncology Group (ECOG) performance status that is either 0 or 1 at screening 6. Must have a leukapheresis material of non-mobilized cells accepted for manufacturing

Exclusion criteria

Exclusion criteria: 1. Prior administration of a genetically modified cellular product including prior BCMA CAR-T therapy. Participants who have received prior BCMA -directed bi-speciific antibodies or anti-BCMA antibody drug conjugate. 2. Prior allogenic stem cell transplantation (SCT) at any time or autologous SCT within 3 months prior to signing informed consent 3. Plasma cell (PC) leukemia and other plasmacytoid disorders, other than MM 4. POEMS syndrome 5. Active central nervous system (CNS) involvement by malignancy 6. Patients with active neurological auto immune or inflammatory disorders

Design outcomes

Primary

MeasureTime frame
Stringent complete response (sCR), complete response (CR), very good partial response (VGPR), partial response (PR), minimal response (MR), stable disease (SD), progressive disease (PD) or unknown (UNK), according to the International Myeloma Working Group (IMWG) criteria.

Countries

Australia, France, Germany, Greece, Italy, Japan, Singapore, Spain

Contacts

Public ContactKyosuke Yamauchi

Novartis Pharma. K.K.

rinshoshiken.toroku@novartis.com+81-120-003-293

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026