Multiple Myeloma · Teclistamab BCMA × CD3 bispecific (with step-up dosing) — continuous SC weekly
Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.
Knowledge-base record for audit. Provisional clinical content: this is not a prescription. An oncologist must verify original sources, applicability and review status. Full rules and constraints are in the YAML.
| Track | aggressive |
|---|---|
| Linked regimen | REG-TECLISTAMAB |
| ID | IND-MM-4L-TECLISTAMAB |
|---|---|
| Type | Indication |
| Status | reviewed 2026-04-25 | pending_clinical_signoff |
| Diseases | DIS-MM |
| Sources | SRC-ESMO-MM-2023 SRC-MAJESTEC-1-MOREAU-2022 SRC-NCCN-MM-2025 |
Notes
STUB — pending Clinical Co-Lead sign-off. Aggressive-track 4L+ option for triple-class refractory MM. Talquetamab (GPRC5D × CD3), elranatamab (BCMA × CD3), cilta-cel + ide-cel CAR-T are alternative modalities — separate future Indications. International referral pathway is dominant access barrier.
Used By
Algorithms
ALGO-MM-2L- ALGO-MM-2LALGO-MM-3L- ALGO-MM-3L
Indication
IND-MM-4L-CILTACEL-CART- IND-MM-4L-CILTACEL-CARTIND-MM-RR-3L-TECLISTAMAB- IND-MM-RR-3L-TECLISTAMAB