Pfizer to Cease Production of Weight Loss Pill’s Twice-Daily Variant

Pfizer to Cease Production of Weight Loss Pill’s Twice-Daily Variant



Pfizer to discontinue twice-daily weight loss pill due to high rates of adverse side effects

Pfizer ⁣announced on Friday that it will​ no longer continue the development of the twice-daily version of its⁤ experimental weight loss pill. This decision comes after obese ⁣patients in a mid-stage⁢ clinical study experienced significant⁣ weight ‍loss but‌ had difficulty tolerating the⁢ drug.​ The study revealed high rates of adverse ‍side effects, mostly mild and gastrointestinal, leading to a significant number of patients discontinuing the drug.

The company⁢ stated, “At this time, twice-daily danuglipron formulation will ​not advance into Phase 3 studies.”

However, Pfizer still plans to release phase two trial data on a once-a-day‍ version of‍ the drug in the first half of 2024. This data⁢ will help ‍determine the next steps⁣ for the drug. Pfizer ⁢will wait ​for the results before deciding whether to proceed with a phase three study on the once-daily pill, which is considered the more⁣ competitive form of the treatment.

Following ‌the announcement of the trial results,⁣ Pfizer’s shares fell 4% in premarket‌ trading on Friday.

For ‍more information, read the full article from www.cnbc.com.

2023-12-01 07:58:31
Article from www.cnbc.com

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