A Placebo-controlled, Double-blind Phase I Study in Healthy Volunteers with IMP761, a LAG-3 Agonist Antibody
Latest Information Update: 29 Jan 2025
At a glance
- Drugs IMP 761 (Primary)
- Indications Autoimmune disorders; Inflammatory bowel diseases; Multiple sclerosis; Rheumatoid arthritis
- Focus Adverse reactions; First in man
- Sponsors Immutep
- 17 Dec 2024 Initial safety data from this study published in the Immutep Limited media release.
- 17 Oct 2024 According to an Immutep Limited media release, company announces that the first part (Part A, single dose) of this study evaluating IMP761 has been fully recruited and the drug has been administered with no safety issues. And now progressed to the Part B dose escalation phase with single IMP761 dosing planned to move from 0.03 mg/kg up to 0.90 mg/kg.
- 25 Sep 2024 According to an Immutep Limited media release, company announces, it has received a fund from research and development (R&D) tax incentive payment in cash from the French Government under its Credit d'Impot Recherche scheme (CIR), funds will be used to support the ongoing and planned global clinical development of eftilagimod alpha and IMP761.