Immutep reports positive interim Phase I data for IMP761
The single ascending dose Phase I met its primary endpoint, showing safety, tolerability and significant pharmacodynamic activity at 7 mg/kg; further updates expected in H2 2026.
See the latest news and media coverage for Immutep. We track all announcements, press releases, and industry mentions in real time, all in one place.
Biotechnology company developing LAG-3 immunotherapies
immutep.comLast updated
In short: Immutep halted its Phase III TACTI-004 lung cancer trial due to futility, while facing a securities class action and a Nasdaq compliance notice.
The single ascending dose Phase I met its primary endpoint, showing safety, tolerability and significant pharmacodynamic activity at 7 mg/kg; further updates expected in H2 2026.
Analysis of 592 patients found increased lymphocyte count linked to improved survival.
Analysis of 5922 patients across five trials shows median OS improvement of 7.7 months in ALC responders.
IDMC recommends halt after futility analysis; root cause under review. IMP761 Phase I advances with favorable safety. Cash at A$110.6M extends to H1 CY2028.
LOS ANGELES, June 15, 2026 /PRNewswire/ -- The DJS Law Group reminds investors of a class action lawsuit against Immutep Limited ("Immutep" or "the Company...
LOS ANGELES, June 8, 2026 /PRNewswire/ -- The DJS Law Group reminds investors of a class action lawsuit against Immutep Limited ("Immutep" or "the Company...
On May 5, 2026, a class action was filed on behalf of all investors who purchased or otherwise acquired Immutep Limited American Depository Receipts (NASDAQ...
First-in-human Phase I study met its primary endpoint, demonstrating favourable safety and tolerability in healthy volunteers in the single...
Track Immutep and your other target companies to get real-time alerts and weekly summaries delivered straight to your inbox.
Browse news for competitors to Immutep and other trending companies.