Copiktra
Named-patient access overview. Copiktra is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
Quick orientation
Copiktra (duvelisib) is an oral dual inhibitor of phosphoinositide 3-kinase delta and gamma (PI3K-delta, PI3K-gamma) marketed by Secura Bio. The US Food and Drug Administration approved Copiktra in September 2018 for adult patients with relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) after at least two prior therapies, and granted accelerated approval for relapsed or refractory follicular lymphoma (FL) after at least two prior systemic therapies (the FL indication was subsequently withdrawn in the US in 2021). Copiktra is dosed at 25 mg orally twice daily in 28-day cycles, with Boxed Warnings for serious infections, diarrhoea or colitis, cutaneous reactions, and pneumonitis. Treatment is initiated and overseen by a haematologist with experience managing PI3K-inhibitor toxicity. Reserve Meds coordinates physician-led cross-border sourcing for international patients.
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How Reserve Meds coordinates Copiktra
- Patient or treating physician submits an intake at the patient portal.
- Reserve Meds clinical team verifies appropriateness for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific named-patient documentation is prepared.
- Copiktra is sourced from a DSCSA-compliant US specialty wholesaler with full serial traceability.
- Shipment is coordinated to the patient's physician or hospital pharmacy with appropriate handling.
Access by country
Reserve Meds publishes a detailed country access guide for Copiktra in every market we coordinate. Each page below covers the destination-country regulatory pathway, real costs, indicative timelines, physician-credential requirements, and handling notes. Tap any country to read the full deep-dive.
Start a request for Copiktra
Submit a 60-second intake. The clinical team will follow up within 24 hours with case-specific feasibility, timeline, and a formal quote.
Frequently asked questions
How can I get Copiktra if it is not approved or available in my country?
Reserve Meds coordinates US-sourced Copiktra for patients through a physician-led, named-patient cross-border pathway. Your treating physician provides the prescription and clinical justification; Reserve Meds prepares the named-patient documentation for your country and arranges DSCSA-compliant US sourcing and delivery to your physician or hospital pharmacy.
Can I access Copiktra through named-patient or compassionate-use import?
Yes. Named-patient access (also called compassionate use or personal import) is the core route Reserve Meds operates for Copiktra. Eligibility and paperwork depend on the regulator in your country, and Reserve Meds maps the specific pathway for each market it coordinates.
Do I need a prescription to access Copiktra through Reserve Meds?
Yes. Reserve Meds is not a pharmacy and does not prescribe. A valid prescription and clinical justification from your treating physician are required, and all clinical decisions remain with your physician.
How does Reserve Meds deliver Copiktra to a patient?
Reserve Meds sources Copiktra from a DSCSA-compliant US specialty supplier with full traceability and coordinates delivery to your treating physician or hospital pharmacy, with appropriate handling for the product.
How long does it take, and what does Copiktra cost through Reserve Meds?
After a short intake, the clinical team responds within one business day with case-specific feasibility, an indicative timeline, and a formal written quote. Cost depends on the destination, the prescribed regimen, and the duration of therapy, and is confirmed in writing before anything proceeds.
How do I start a request for Copiktra?
Submit a 60-second intake through the Reserve Meds patient portal, or message the concierge team on WhatsApp. A named coordinator follows up within 24 hours.