Icotrokinra ‘best in class oral therapeutic for plaque psoriasis’

The phase 3 ICONIC-LEAD study showed​ that icotrokinra, a peptide drug that blocks the interleukin (IL)-23 receptor, was able to induce significant clearance of psoriatic plaques.

The drug is being developed in conjunction with Johnson & Johnson and Protagonist will earn $115 million as a milestone payment from the big pharma for successful completing a phase 3 study.

Protagonist has already earned $35 million due to acceptance of an NDA in psoriasis and $15 million for starting a phase 3 study in a second indication bringing its total milestone payments up to $165 million.

The IGA scale is used to measure severity of psoriasis and ranges from 0 to 4, where 0 is clear skin and 4 indicates severe disease. The results from the trial show 65% of patients were able to achieve clear skin (an IGA score of 0 or 1) at week 16 versus only 8% of the placebo group.

The PASI score relates to the amount of surface area on each part of the body that is covered by psoriasis plaques and also grades severity of the plaques. A score of 90 or more means that this has improved by 90% from the start of the study, which 50% of icotrokinra patients achieved versus only 4% of the placebo group.

The effects of the drug improved with time and by week 24, 74% of patients had achieved clear skin and 65% achieved PASI90. Around 49% of people in the treatment and placebo group had some form of adverse event, showing no increase with icotrokinra treatment.

“These positive phase 3 results confirm the compelling efficacy and safety trends that were observed with the previous Phase 2b FRONTIER-1 and -2 studies, highlighting icotrokinra’s potential as a best-in-class oral agent providing an ideal combination of significant skin clearance with demonstrated tolerability in a once-daily pill for treating plaque psoriasis,” said Dinesh Patel, President and CEO of Protagonist.

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