Drug data last refreshed 17h ago · AI intelligence enriched 1w ago
RISVAN is a long-acting intramuscular suspension formulation of risperidone, a second-generation antipsychotic, approved in March 2024. Risperidone is indicated for schizophrenia, bipolar disorder, and irritability associated with autism spectrum disorder. The extended-release formulation improves treatment adherence by reducing injection frequency compared to oral antipsychotics.
Recent market entry in growth phase with strong patent protection through 2031 suggests expanding commercial teams and increasing promotional activity.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Safety, Tolerability, and Pharmacokinetics of Switching From Oral Risperidone to Risperidone Implant
Safety, Tolerability, Pharmacokinetics and Efficacy of 180 mg Subcutaneous Risperidone From 6 mg Oral Risperidone
A Study to Evaluate the Ability of Conducting a Study of Oral Risperidone Followed by Paliperidone Palmitate in Rwandan Healthcare Facilities
Mirror-image Study of Paliperidone Palmitate and Risperidone Long-acting Injection
Comparison of the Effectiveness of Brexpiprazole With That of Risperidone
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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RISVAN represents a growth-stage product launch opportunity for professionals seeking to build a brand from market entry through peak sales. The 4.7-year exclusivity window and competitive market require strong sales execution, physician relationships, and payer strategy.