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Palatin Loses Sexual (Dysfunction) Partner

 
• By Lisa LaMotta

Just weeks after the approval of the first female sexual dysfunction drug, a competitor is facing problems with its own treatment for the issue. Palatin Technologies announced its partner, Gedeon Richter, has decided to part ways and return the drug back to Palatin.

The pair signed a licensing agreement for bremelanotide in August 2014 for co-development and commercialization in the EU. Palatin received $9.8m in upfront payments, as well as $3.1m in milestone...

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GlycoEra’s Series B Cash Will Fund Efforts To Take On FcRn Inhibitor Class

 
• By Joseph Haas

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Merck KGaA Plans Phase III For Enpatoran After Mixed Phase II Lupus Data

 
• By Jessica Merrill

The Phase II study testing the novel TLR7/8 inhibitor met the primary endpoint in a cohort of patients with cutaneous lupus erythematosus and systemic lupus erythematosus with rash, but did not in patients with SLE.

Merck & Co. CMO Barr On Breaking Into Immunology And Ophthalmology

 
• By Jessica Merrill

Chief medical officer Eliav Barr discussed Merck’s investment in new therapeutic areas and business development in an interview with Scrip.

J&J’s Imaavy Approval Is The Starting Line For Pipeline-In-A-Product Strategy

 
• By Jessica Merrill

The company’s FcRn inhibitor nipocalimab was approved by the US FDA for generalized myasthenia gravis (gMG), where it will join a competitive market.

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Gilead Ready To Go After Hepatitis D Again

 
• By Joseph Haas

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Progress In The Effort To Improve Outcomes In SCLC

 
• By Jessica Merrill

Several drug makers are working to bring new advances to small-cell lung cancer, a fast-growing cancer with limited treatment options.

GSK’s Nucala Set For Dupixent Face-Off After FDA COPD Nod

 
• By Kevin Grogan

The UK major's asthma drug gets a key expanded approval.