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Immutep Limited (IMMP)

NasdaqGM - NasdaqGM Real Time Price. Currency in USD
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2.1700+0.0400 (+1.88%)
At close: 04:00PM EDT
2.1800 +0.01 (+0.46%)
After hours: 06:16PM EDT
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Trade prices are not sourced from all markets
Previous Close2.1300
Open2.1400
Bid2.1400 x 400
Ask2.1800 x 400
Day's Range2.1200 - 2.1800
52 Week Range1.5800 - 3.3400
Volume102,360
Avg. Volume403,996
Market Cap325.958M
Beta (5Y Monthly)1.90
PE Ratio (TTM)N/A
EPS (TTM)-0.2000
Earnings DateJul 28, 2024 - Aug 01, 2024
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est8.01
  • GlobeNewswire

    Immutep Announces Successful Meeting with FDA on Phase III Design in Non-Small Cell Lung Cancer

    Media Release Final discussion with the FDA, successfully concluding the regulatory preparations for the TACTI-004 Phase III trial design to evaluate efti in combination with KEYTRUDA® (pembrolizumab), MSD’s anti-PD-1 therapy, and standard chemotherapy in first-line non-small cell lung cancerTACTI-004 registrational trial will enrol ~750 patients regardless of PD-L1 expression in order to address the entire 1L NSCLC market eligible for anti-PD-1 therapy SYDNEY, AUSTRALIA, July 22, 2024 (GLOBE NE

  • GlobeNewswire

    Immutep Receives Regulatory Clearance for Phase I Study of First-in-Class LAG-3 Agonist Antibody Designed to Treat Autoimmune Diseases

    Media Release Study expected to enrol first participants during Q3 CY2024 SYDNEY, AUSTRALIA, July 17, 2024 (GLOBE NEWSWIRE) -- Immutep Limited (ASX: IMM; NASDAQ: IMMP) ("Immutep” or “the Company”), a clinical-stage biotechnology company developing novel LAG-3 immunotherapies for cancer and autoimmune disease, today announces it has received regulatory clearance from the ethics and competent authority in the Netherlands to initiate the first-in-human Phase I study of IMP761. IMP761 is the world’s

  • Zacks

    Immutep (IMMP) Up as Combo Therapy Meets Carcinoma Study Goals

    Immutep (IMMP) jumps 15% on positive results from a late-stage study evaluating its candidate, efti, in combination with Keytruda to treat first-line head and neck squamous cell carcinoma patients.