0.00Open0.30Pre Close0 Volume160 Open Interest5.00Strike Price0.00Turnover0.00%IV169.72%PremiumJan 17, 2025Expiry Date0.00Intrinsic Value100Multiplier-7DDays to Expiry0.30Extrinsic Value100Contract SizeAmericanOptions Type--Delta--Gamma6.55Leverage Ratio--Theta--Rho--Eff Leverage--Vega
Immutep Stock Discussion
Patient Enrolment Completed for EFTISARC-NEO Phase II Trial
Wednesday, 22nd January at 8:00 am
Phase II trial evaluating efti in combination with radiotherapy plus KEYTRUDA® (pembrolizumab) in patients with soft tissue sarcoma reaches enrolment target of 40 patients
Data updates from EFTISARC-NEO expected in 2025
SYDNEY, AUSTRALIA, Jan. 22, 2025 (GLOBE NEWSWIRE) -- Immutep Limited ((ASX: IMM, NASDAQ: IMMP) ("Immutep" or "the Company"), a clinical-stage biotechnology co...
INSIGHT-003 is an investigator-initiated study led by the Frankfurt Institute of Clinical Cancer Research IKF evaluating a triple combination therapy in first-line non-small cell lung cancer patients.
It is testing eftilagimod alpha in combination with antiPD-1 therapy, pembrolizumab, and doublet chemoth...
Immutep and Monash University Announce First Publication Detailing How Human LAG-3 Binds to MHC Class II
Monday, 16th December at 8:00 am
• Findings published in Science Immunology resolve how human LAG-3 binds to its main ligand providing a better foundation for development of blocking LAG-3 therapeutics, including Immutep's anti-LAG-3 small molecule program
• Data also supports eftilagimod alfa's (efti) preferential binding to a subset of MHC Class II molecules on anti...
Immutep Reports Promising New Data in Head and Neck Cancer at ESMO Immuno-Oncology 2024
Immutep (NASDAQ: IMMP) has announced promising clinical results from Cohort B of the TACTI-003 Phase IIb trial, evaluating eftilagimod alpha (efti) combined with KEYTRUDA® in head and neck cancer patients. The study shows significant improvements in patients with PD-L1 CPS <1 expression, including:
- Median overall survival (OS) not yet reached with 67% 12-month OS rate
- Progression-fr...
“The receipt of regulatory approval from the Australian Therapeutic Goods Administration t...
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