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Available at: Accessed August 31, 2013

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Meanwhile, on the novel biologics front, it initiated Phase I clinical trials for one candidate and pre-clinical studies for another candidate in India

Has the FDA issued a final decision affecting the substance, or is the status based only on the July 2026 advisory vote

The FDA recommends using a non-oral or additional barrier method for 4 weeks after tirzepatide initiation and for 4 weeks after each dose increase

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