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INVEGA SUSTENNA®

(paliperidone palmitate)

This information is intended for US healthcare professionals to access current scientific information about J&J Innovative Medicine products. It is prepared by Medical Information and is not intended for promotional purposes, nor to provide medical advice.

INVEGA SUSTENNA - Conversion to INVEGA SUSTENNA - From Long-Acting Injectable Antipsychotics

Last updated : 11/11/2024

SPECIFIC RESPONSE

When switching patients currently at steady-state on a long-acting injectable antipsychotic, initiate INVEGA SUSTENNA therapy in place of the next scheduled injection. INVEGA SUSTENNA should then be continued at monthly intervals. The one-week initiation dosing regimen (234 mg on day 1 and 156 mg one week later) is not required.1

Switching From RISPERDAL CONSTA to INVEGA SUSTENNA

Doses of RISPERDAL CONSTA and INVEGA SUSTENNA Needed to Attain Similar Levels of Active Moiety Exposure at Steady State2

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Formulation

RISPERDAL CONSTA

INVEGA SUSTENNA

Dosing Frequency

Every 2 weeks

Once every 4 weeks

Dose

12.5 mg

39 mg

25 mg

78 mg

37.5 mg

117 mg

50 mg

156 mg

Plasma concentrations of the active moiety are maintained close to steady-state concentrations after the switch from RISPERDAL CONSTA to INVEGA SUSTENNA. No oral supplementation is required during the switch in treatment.2

Clinical Rationale

Results from PK modeling simulations suggest that patients previously stabilized on RISPERDAL CONSTA can attain similar levels of active moiety steady-state exposure during maintenance treatment with specific monthly doses of INVEGA SUSTENNA.2

PK, pharmacokinetic.

References

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1. INVEGA SUSTENNA [(paliperidone palmitate) Extended-Release Injectable Suspension] [Prescribing Information]. Titusville, NJ: Janssen Pharmaceuticals, Inc; https://imedicalknowledge.veevavault.com/ui/approved_viewer?token=7994-54c7ff1c-5e50-4845-a605-24e8c5104cd7.

2. Johnson & Johnson Pharmaceutical Research and Development: Raritan, NJ; DoF; 2009.