Taisho Makes Japan Vornorexant Filing, Hopes To Dent Insomnia Market

Potential Half-Life Advantage

Taisho’s in-house insomnia therapeutic candidate vornorexant offers a potential advantage of a shorter half-life compared to its competitors, which can contribute to patients’ QOL.

Taisho filed for vornorexant's global first approval in Japan.
Taisho files vornorexant's for global first approval in Japan. • Source: Shutterstock

Taisho Pharmaceutical Co., Ltd. has filed for the global first approval of its in-house oral dual orexin 1 and 2 receptor antagonist (DORA), vornorexant (development code TS-142), for insomnia in Japan. It marks the first such filing from the Japanese OTC giant's in-house pipeline since the firm announced a business restructuring with an enhanced focus on new drug development.

The Japanese firm noted that the candidate comes with a shorter half-life compared to other DORA competitors, which can

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