Why Is Cancer-Focused Immatics Stock Trading Lower On Thursday?

Zinger Key Points
  • The Phase 3 trial for IMA203 in melanoma patients is expected to start in December 2024, with full FDA approval submission planned for 2027.

On Thursday, Immatics N.V. IMTX stock is trading lower after the company commenced an underwritten public offering of $150 million.

The company also announced updated Phase 1b data on ACTengine IMA203 TCR-T targeting PRAME in melanoma patients and provided an update on SUPRAME, the upcoming Phase 3 trial to evaluate IMA203 in metastatic melanoma patients.

As of August 23, 2024, 28 heavily pretreated patients with metastatic melanoma were treated with IMA203 at the recommended Phase 2 dose (RP2D, 1 to 10 billion total TCR-T cells) during the Phase 1b dose expansion part of the clinical trial.

IMA203 monotherapy has maintained a favorable tolerability profile with no treatment-related Grade 5 adverse events in the safety population, even at doses up to ~10×10 power 9 TCR-T cells.

The data presented demonstrate a significant positive shift in median progression-free survival (PFS) and median overall survival (OS) between melanoma patients treated during Phase 1a and patients treated in Phase 1b.

In addition, approximately half of all patients in the Phase 1b trial have a deep response (>50% tumor reduction).

This subgroup of patients was observed to have a median PFS of more than one year, while patients with <50% tumor reduction (including patients with tumor size increase) were still observed with a more than 2 times longer median PFS compared to patients treated in dose escalation with suboptimal doses.

Translational data from patients across Phase 1a and Phase 1b indicate that IMA203 T cells rapidly engrafted in all patients after a single dose and show a persistence of more than two years.

The Phase 3 trial will evaluate IMA203 targeting PRAME in 360 HLA-A*02:01-positive patients with second-line or later unresectable or metastatic melanoma.

The Phase 3 trial is on track to commence in December 2024 and patient enrollment is forecasted to be completed in 2026. A pre-specified interim analysis is planned for early 2026.

The company aims to submit an FDA marketing application in early 2027 for full approval.

Price Action: IMTX stock is down 11.1% at $9.841 at last check Thursday.

Photo via Shutterstock

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