Pleconaril for extemporaneous preparation

Scope of information

This information is intended for healthcare professionals and institutional or authorised customers only.

All technical, quality-, and supply‑related information referenced on this page is made available to authorised recipients upon request.

Background

Pleconaril was previously developed by Apodemus/Curovir as an investigational medicinal product.

In recent years, the company has received unsolicited enquiries from healthcare professionals regarding access to pleconaril for use in individual patients, in situations where no commercially authorised alternative is available.

In response to such enquiries, pleconaril is supplied as a Good Manufacturing Practice (GMP)–manufactured active pharmaceutical ingredient (API) for extemporaneous preparation by qualified healthcare professionals. Any such use is under the responsibility of the prescribing physician and must be conducted in accordance with applicable national and local requirements.

The material is provided to support professional access to pleconaril as an API and does not constitute promotion of a medicinal product.

Scientific background

Information on the scientific background of pleconaril is available in the published literature and may be discussed with healthcare professionals upon request.

Quality and supply

Pleconaril is manufactured under GMP and supplied as an API for use in extemporaneous preparation.

Formulation and analysis

Technical information relating to formulation and analytical methods is available as part of the standard quality documentation.

Stability

Pleconaril is supported by long‑term stability data generated in accordance with GMP, enabling storage over extended periods. This supports procurement and stockholding by healthcare institutions for potential future patient needs and preparedness.

Batch‑specific quality and stability information is provided as part of the standard quality documentation.

Availability

Pleconaril is available in 30 g bottles appropriate for patient‑specific extemporaneous preparation.

For further information regarding availability and supply terms, please contact: info@curovir.com

Important information

This information is intended for healthcare professionals and institutional customers only.

Pleconaril is supplied as an active pharmaceutical ingredient (API) manufactured in compliance with Good Manufacturing Practice (GMP) for use in extemporaneous preparation. Pleconaril is not supplied as a finished medicinal product.

Any clinical use is at the sole discretion and responsibility of the treating healthcare professional and must comply with all applicable local laws, regulations, ethical standards, and institutional requirements.

No therapeutic, efficacy, or safety claims are made. Nothing on this website should be construed as medical advice, a treatment recommendation, or an encouragement to prescribe or use pleconaril.