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The median follow-up time after delivery was 26.3 months (range, 12 to 142 months)

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International Regulatory Status Regulatory classification varies significantly by jurisdiction: Approved as pharmaceutical in Russia and select Commonwealth of Independent States (CIS) countries for generalized anxiety disorder Not authorized as medicine in European Union member states Unavailable through regulatory channels in United Kingdom, Canada, and Australia Often marketed as research chemical in jurisdictions without explicit prohibition WADA Status Current World Anti-Doping Agency classification: Selank does not appear on the current WADA Prohibited List as of 2025 However, could potentially fall under Section S0 (Non-Approved Substances) depending on interpretation Lack of widespread regulatory approval may create ambiguity for competitive athletes Athletes should verify current status with national anti-doping organizations before use Research Classification: Selank is available for laboratory research use only in most jurisdictions