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Our Pipeline:

About PRAME

PRAME is a target expressed in more than 50 cancers. Immatics is the global leader in precision targeting of PRAME and has the broadest PRAME franchise with the most PRAME indications and modalities.

Immatics’ PRAME franchise includes multiple product candidates, therapeutic modalities, indications and combination approaches: anzu-cel (anzutresgene autoleucel; IMA203) and IMA203CD8, both PRAME-directed cell therapies, and IMA402, a PRAME-directed bispecific. Combination approaches include IMA402 with immune checkpoint inhibitors, IMA402 with the MAGEA4/8-directed bispecific IMA401, and anzu-cel in combination with Moderna’s PRAME mRNA therapy designed to enhance the cell therapy response.

Pipeline

Preclinical
Phase 1a
Dose escalation
Phase 1b
Dose expansion
Phase 2
Phase 3
Product Candidate Anzu-cel (IMA203)
SUPRAME
Modality
Cell Therapy
Target
PRAME
Indication
2L melanoma, patients with unresectable or metastatic melanoma who have received at least 1 prior immune checkpoint inhibitor
Product Candidate Anzu-cel (IMA203)
Modality
Cell Therapy
Target
PRAME
Indication
Uveal melanoma
ANZU-CEL (IMA203) + MRNA-4203
Modality
Cell Therapy
Target
PRAME
Indication
Solid Cancers
IMA203CD8
Modality
Cell Therapy
Target
PRAME
Indication
Gynecologic cancers, other solid cancers
IMA402
Modality
Bispecific
Target
PRAME
Indication
Melanoma, gynecologic cancers and others
IMA402 + ICI
Modality
Bispecific
Target
PRAME
Indication
Melanoma, gynecologic cancers and others
IMA402 + IMA401
Modality
Bispecific
Target
PRAME, MAGEA4/8
Indication
sqNSCLC
IMA401 WITH OR WITHOUT CHECKPOINT INHIBITOR (PEMBROLIZUMAB)
Modality
Bispecific
Target
MAGEA4/8
Indication
HNSCC, sqNSCLC and others
UNDISCLOSED
Modality
Bispecific
Target
Undisclosed
Indication
other

The PRAME franchise

3
Product candidates
2
Therapeutic modalities
3
Combination Therapies
Female patient smiling in their home

Clinical trials

Immatics is evaluating its targeted PRAME cell therapies and bispecific product candidates and actively enrolling patients in ongoing clinical trials.