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The time and financial pressures drug development teams face is immense, and when factoring in failures and capital expenditures, the cost to develop a new drug increases fivefold

This page draws from regulatory sources, clinical-trial registries, peer-reviewed studies, PubMed-indexed literature, and scientific databases

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Dihexa or its analogs were administered 5 minutes after scopolamine, either intracerebroventricularly at doses of 0.1 or 1 nmol), intraperitoneally at doses of 0.05, 0.25, or 0.50 mg/kg, or orally at doses of 1.25 or 2.0 mg/kg

MECHANISM CATEGORIES SAFETY Side effects Generally well-tolerated in trials at the doses tested Injection-site reactions Known interactions Not characterized in Phase 3 Contraindications Pregnancy/lactation (unstudied) REGULATORY STATUS FDA Not FDA-approved as a drug

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