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The designation is supported by the positive outcomes from the double-blind Phase III HERCULES trial, where the therapy showed a 31% delay in the time to onset of

This initiative is facilitated through a Named Patient Program (NPP), allowing patients to access these treatments based on clinical evidence and medical needs prior to regulatory approval. The

The total funding is set to amount to $9.1m and the initial research grant of $1m was announced in January this year. The additional funding from RSRT will

With this financing round, the company’s total funding reached more than $25m. Small molecule drugs developed by the company specifically target viral proteins crucial to the polyomavirus life

Acromegaly is a serious disease which is generally caused by a benign pituitary adenoma. Paltusotine would be the first, once-daily, oral selective somatostatin receptor type 2 nonpeptide agonist

TO-208, known as VP-102 in the US and marketed under the brand name YCANTH, contains cantharidin as its active ingredient. A Phase III clinical trial was conducted in

This designation marks the beginning of the UK Innovative Licensing and Access Pathway (ILAP), which is designed to expedite the development and access of new medicines in the

This move grants Theratechnologies the ‘rights’ to potentially introduce treatments for familial chylomicronaemia syndrome (FCS), hereditary angioedema (HAE), and severe hypertriglyceridemia (sHTG) within the Canadian market. Under the

The single-asset focused partnership leverages Tubulis’ platforms, Tubutecan and Alco5, to create an ADC with stability and reduced off-target toxicity, addressing present treatment challenges. Under the agreement terms,