IMCR Immunocore Holdings plc

BULLISH Impact: 6/10 PRESS-RELEASE
Horizon months Filed May 31, 2026 Processed 13d 1h ago Wire GlobeNewswire
Press release: announcement
Latest settled — T+5d
IMCR ▼ -2.88% at T+5d
LONG call ✗ call lost -2.88% · α vs SPY -0.13% · entry $29.13 → $28.29
Next anchor: T+20d in 16d
Currently $28.96 · -0.58% from $29.13 entry
Entry anchored
May 31, 2026
via day open
T+1d
+1.48%
call +1.48% · α +1.33%
$29.56
settled 12d ago
T+5d
-2.88%
call -2.88% · α -0.13%
$28.29
settled 8d ago
T+20d
call — · α —
in 16d
T+60d
call — · α —
in 2mo

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Executive Summary

Immunocore presented updated Phase 1 data for brenetafusp in heavily pretreated advanced melanoma at ASCO 2026, showing a 6-month OS rate of 87% and DCR of 52% in 66 patients. The data support the 160 mcg dose selection for the ongoing Phase 3 PRISM-MEL-301 trial in first-line advanced melanoma. While the results are clinically promising, the small sample size and early-stage nature limit immediate stock-moving impact.

Actionable Insight

The Phase 1 data are encouraging but early-stage; the key catalyst is the Phase 3 PRISM-MEL-301 trial readout. Monitor for enrollment updates and interim data. The stock may see modest positive movement on ASCO presentation buzz, but sustained upside depends on Phase 3 results.

Key Facts

  • Brenetafusp monotherapy in 66 heavily pretreated advanced melanoma patients showed 6-month OS rate of 87% and median OS of 14.3 months.
  • Disease control rate (DCR) was 52% and overall response rate (ORR) was 12%.
  • Data support 160 mcg dose selection for Phase 3 PRISM-MEL-301 trial (brenetafusp + nivolumab vs. standard nivolumab regimens) in first-line advanced melanoma.
  • Clinical benefit was consistent across difficult-to-treat subgroups, including patients with primary PD-1 resistance (median OS 14.7 months).
  • Brenetafusp was generally well tolerated; most common TRAEs were CRS (56%), rash (44%), pyrexia (44%), and chills (38%), predominantly low grade.
  • A second poster showed IL7 may enhance ImmTAC anti-tumor activity in vitro and in vivo.

Financial Impact

No financial data provided; early-stage clinical data with no revenue or guidance impact.

Risk Factors

  • Phase 3 trial may fail to replicate Phase 1 efficacy in a larger, randomized setting.
  • Competition from existing PD-1/CTLA-4 and LAG-3 therapies in first-line melanoma.
  • Safety profile includes CRS and lymphopenia, which could limit tolerability in broader patient populations.
  • Small sample size (n=66) limits statistical reliability of efficacy estimates.

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
78% bullish (23 analysts)

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3303917
5 reports for IMCR
Performance horizon

Track record builds as more directional reports settle.

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Reports for IMCR — sortable, filterable
Type Now
May 31, 2026
13d ago
Press Release
BULLISH ★ 6/10
$29.13 $28.29▼ −2.88%▼ −0.13%$28.96 (−0.58%)
Apr 19, 2026
7w ago
Press Release
BULLISH ★ 8/10
$31.46 $28.56▼ −9.22%▼ −10.13%$28.96 (−7.95%)
Apr 8, 2026
9w ago
144
NEUTRAL ★ 3/10
$31.85 $31.64▼ −0.66%▼ −4.18%$28.96 (−9.07%)
Mar 17, 2026
12w ago
Press Release
NEUTRAL ★ 5/10
$30.04 $30.28▲ +0.80%▲ +1.51%$28.96 (−3.60%)
Feb 25, 2026
15w ago
8-K
BULLISH ★ 7/10
$32.16 $33.73▲ +4.88%▲ +5.98%$28.96 (−9.95%)
Showing 5 of 5

US Market Status

Market Closed — Opens Mon (48h 2m)

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