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6-K ·Filed May 1, 2026

PRRUF

IMMUTEP Ltd
BEARISH
Impact 8/10
Horizonimmediate Processed5mo ago SEC0001193125-26-201355
Notable filing: 6-K
Actionable Insight ▼ Bearish

Expect significant share price decline on the Phase III failure. Monitor root cause analysis results and any updates on efti program viability. The company's cash runway and cost cuts provide some buffer, but the lead program's failure introduces substantial uncertainty.

DirectionBearish
Confidencehigh
Horizonimmediate
Final — all horizons settled through T+60d
PRRUF ▲ 0.00% at T+60d
SHORT call ✗ call lost 0.00% · α vs SPY +3.07% · entry $0.0500 → $0.0500
Entry = T+0 close
May 1, 2026
via day close
T+1d
0.00%
call 0.00% · α -0.34%
$0.0500
settled 6mo ago
T+5d
0.00%
call 0.00% · α +2.35%
$0.0500
settled 6mo ago
T+20d
0.00%
call 0.00% · α +5.28%
$0.0500
settled 5mo ago
T+60d
0.00%
call 0.00% · α +3.07%
$0.0500
settled 3mo ago

Price Chart

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Executive Summary

Immutep reported discontinuation of its lead TACTI-004 Phase III trial for eftilagimod alfa in first-line non-small cell lung cancer following an IDMC futility analysis. The efti arm underperformed the control arm, prompting a wind-down and root cause analysis that may impact the broader efti program. The company has a cash position of A$110.6 million but faces a US$10 million payment obligation to partner Dr. Reddy's, and has initiated cost reductions including headcount cuts.

Key Facts

  • TACTI-004 Phase III trial discontinued after IDMC interim futility analysis showed efti arm underperformed control arm in 1L NSCLC
  • Root cause analysis ongoing; implications for efti development program under review
  • Immutep must pay US$10 million to Dr. Reddy's by June 2026 due to trial discontinuation
  • Cash, cash equivalents, and term deposits total A$110.6 million as of March 31, 2026
  • Cash used in R&D activities was A$11.8 million in Q3 FY26
  • Cost reduction measures initiated, including targeted headcount reduction
  • IMP761 Phase I trial progressing to multiple ascending dose phase; data expected at EULAR June 2026
  • EFTISARC-NEO Phase II met primary endpoint; FDA orphan drug designation received
  • Net cash from operating activities was A$13.5 million in Q3 FY26, driven by Dr. Reddy's upfront payment

Financial Impact

Material – TACTI-004 discontinuation erodes pipeline value; US$10 million cash outflow to Dr. Reddy's due in June 2026; cash position of A$110.6 million provides runway into H1 CY2028; no revenue or EPS reported

cashpipeline valuepotential future revenue

Risk Factors

  • Root cause analysis may reveal broader issues with efti, leading to program discontinuation
  • Potential need for additional financing if cash burn accelerates or milestones are missed
  • Reliance on Dr. Reddy's partnership; further obligations or changes in collaboration terms

Market Snapshot

Exchange
OTC
Sector
Pharmaceutical Preparations
Analyst Consensus
50% bullish (8 analysts)

Investment Themes

Documents Analyzed

This report is based on 5 SEC documents filed with EDGAR.

DocumentAccession Number
6-K Filing (Primary)0001193125-26-201355
Document: d70756d6k.htm0001193125-26-201355
Document: 0001193125-26-201355-index-headers.html0001193125-26-201355
Document: 0001193125-26-201355-index.html0001193125-26-201355
Document: 0001193125-26-201355.txt0001193125-26-201355
2 reports for PRRUF
Performance horizon
Filters
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Reports for PRRUF — sortable, filterable
TypeNow
May 1, 2026
25w ago
6-K
BEARISH ★ 8/10
$0.0500 $0.0500· 0.00%▲ +3.07%$0.0200 (+60.00%)
Apr 1, 2026
29w ago
3
NEUTRAL ★ 3/10
$0.0400 $0.0500▲ +25.00%▲ +11.62%$0.0200 (−50.00%)
Showing 2 of 2

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Report published May 1, 2026