Immutep and Dr. Reddy's Laboratories have inked an exclusive licensing pact granting Dr. Reddy's rights to develop and commercialize eftilagimod alfa (efti) outside North America, Europe, Japan, and Greater China. Immutep secures $20M upfront, up to $349.5M in milestones, and double-digit royalties, retaining manufacturing control.
Immutep SAS and Dr. Reddy's Laboratories SA announced a strategic collaboration on December 8, 2025, for eftilagimod alfa, a first-in-class immunotherapy activating antigen-presenting cells to fight cancer via LAG-3 and MHC Class II mechanisms. Efti targets solid tumors, headlining a Phase III trial (TACTI-004/KEYNOTE-F91) for first-line non-small cell lung cancer (NSCLC) with pembrolizumab and chemotherapy, plus studies in head & neck cancer, breast cancer, and sarcoma. Immutep retains rights in premium markets and global manufacturing, supplying Dr. Reddy's for emerging regions.
Key Highlights
Financials: $20M upfront (~AUD 30.2M) to Immutep; up to $349.5M (~AUD 528.4M) in milestones; double-digit royalties on sales.
Territory: Exclusive to Dr. Reddy's in all countries excluding North America, Europe, Japan, Greater China.
Exec Quotes: "Ideal partner to maximize impact," says Immutep CEO Marc Voigt; "New standard of care potential," notes Dr. Reddy's M.V. Ramana.
Pipeline Momentum: FDA Fast Track for NSCLC/HNSCC; favorable safety for combos with PD-1 therapy, chemo, radiation.
Sources: GlobeNewswire (Immutep Release), Express Pharma, Economic Times.