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Sanofi abandons plan to seek approval for eczema drug from $1.1B Kymab buyout

Sanofi halts development of a key eczema treatment derived from its Kymab acquisition following a recent pipeline review.

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The brief

Sanofi is discontinuing the development of the OX40L antibody amlitelimab, originally acquired through its purchase of Kymab. The decision follows a broad review of the pharmaceutical company's drug pipeline conducted under the leadership of its new CEO.

Coverage from BioSpace, Endpoints News, FirstWord Pharma, WSJ, and Fierce Biotech emphasizes that this shift marks a significant change for the Kymab-related assets. Reports vary on the valuation of the initial buyout, citing figures between $1.1 billion and $1.4 billion.

Future updates will depend on further disclosures regarding the impact of the pipeline review on Sanofi’s remaining drug candidates. Coverage does not yet specify the long-term strategic adjustments expected under the company's new management.

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Quick answers

What drug is being discontinued?

Sanofi is shelving amlitelimab, an OX40L antibody intended for atopic dermatitis.

Why is the project being canceled?

The cancellation follows a pipeline review conducted under Sanofi's new CEO.

What was the cost of the Kymab acquisition?

Reports vary, with sources citing both $1.1 billion and $1.4 billion.

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