Dr Reddy’s inks licensing deal to sell Immutep’s cancer drug

Dr Reddy’s has signed an exclusive licensing deal with Australia’s Immutep to make, develop and distribute the company’s cancer treatment, according to a stock exchange filing on Monday.

The agreement, worth up to almost $350 million, gives Dr Reddy’s the right to distribute eftilagimod alfa, Immutep’s cancer therapy, in all regions except North America, Europe, Japan and Greater China.

Efti is Immutep’s first-in-class immunotherapy that directly activates the immune system to fight cancer. It is being tested in TACTI-004 (KEYNOТЕF91), a Phase III trial for first-line treatment of advanced or metastatic non small cell lung cancer. Efti is also being studied for other uses, including head and neck cancer, breast cancer and soft tissue sarcoma.

Dr Reddy’s shares swung between gains and losses on BSE Sensex in initial trade, before plunging to day’s low of Rs 1267.50 a piece.

Under the licensing deal, Immutep will receive major milestone payments and can retain a large share of future gains in the licensed markets as efti moves towards commercial use. Immutep will also keep global manufacturing rights for the drug and will supply it to Dr Reddy’s in the licensed regions, while keeping full rights in the key markets of North America, Europe and Japan.

As part of the agreement, Immutep will get an upfront payment of $20 million from Dr Reddy’s. It may also receive further regulatory, development and commercial milestone payments of up to $349.5 million, along with double- digit royalties on future sales in these markets, Dr Reddy’s said in exchange filing.

“This collaboration marks our continuous efforts to deliver first-in-class and innovative therapies for cancer treatment. Efti is a novel immunotherapy with the potential to set a new standard of care in combination with pembrolizumab (Keytruda) and chemotherapy as first-line therapy for non small cell lung cancer,” said M.V. Ramana, CEO – Branded Markets (India & Emerging Markets), Dr. Reddy’s.

Related Posts

LB Pharma Begins Pivotal Phase 3 Schizophrenia Trial

Phase 2 results for LB-102 showed statistically significant reductions in PANSS total score across all doses with onset by week 1 and sustained through study end, alongside low rates of…

Check manufacturing, sale of 26 unapproved drugs, central regulator tells state authority

After substandard drug manufacturing, the state drug firms are once again under the scanner of the central government for manufacture and sale of unapproved fixed dose combination (FDC) drugs which…

Leave a Reply

Your email address will not be published. Required fields are marked *

You Missed

LB Pharma Begins Pivotal Phase 3 Schizophrenia Trial

LB Pharma Begins Pivotal Phase 3 Schizophrenia Trial

Check manufacturing, sale of 26 unapproved drugs, central regulator tells state authority

Check manufacturing, sale of 26 unapproved drugs, central regulator tells state authority

Stem cell therapy for autism illegal: NMC advisory

Stem cell therapy for autism illegal: NMC advisory

India’s Essential Medicines Prices To Increase Marginally From 1 April Under Annual Pricing Framework

India’s Essential Medicines Prices To Increase Marginally From 1 April Under Annual Pricing Framework

Delhi HC Asks Dr Reddy’s To Halt Olymviq Sales; Flags Similarity With Novo Nordisk’s Ozempic

Delhi HC Asks Dr Reddy’s To Halt Olymviq Sales; Flags Similarity With Novo Nordisk’s Ozempic

NPPA allows 0.64% hike in MRP of essential drugs in line with WPI rise

NPPA allows 0.64% hike in MRP of essential drugs in line with WPI rise