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Manufacturer / Innovator:
USA
Regulatory Approval:
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Medicines sourced from authorized manufacturers with full batch traceability.
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Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.
Daybue (trofinetide) is a synthetic peptide, the first FDA-approved treatment specifically for Rett syndrome. It is indicated for:
Daybue is a prescription medicine and must be used under the supervision of a qualified pediatric neurologist or specialist experienced in treating Rett syndrome.
Taken orally or via gastrostomy tube, morning and evening, with or without food.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
Step 1 – Search & request your medicine: The patient or treating doctor submits a request with basic details to initiate the access process.
Step 2 – Verification & eligibility review: The team verifies availability and reviews eligibility against regulatory and clinical requirements to ensure a compliant pathway.
Step 3 – Receive quote & delivery timeline: A transparent quotation is shared, covering medicine cost, logistics, and a clear delivery timeline.
Step 4 – Regulatory approval process: Assistance is provided to secure the approvals and documentation required for legal cross-border access.
Step 5 – Temperature-controlled import & handling: The medicine is sourced and transported under strict GDP-compliant, cold-chain conditions to maintain product integrity.
Step 6 – Secure delivery: The medicine is delivered to the patient or treating hospital, with updates provided at each stage.
Note: From request to delivery, every step is designed to ensure your treatment reaches you safely, compliantly, and without unnecessary delays.
Daybue (trofinetide) oral solution may be imported in the patient's name only, by patients or government hospitals, in line with India's import regulations for unapproved medicines. The following documentation is required:
The order is confirmed only after receipt and verification of a valid prescription from the doctor and, if applicable, an import permit.
Daybue (trofinetide oral solution) is a prescription medicine that legally requires a doctor's prescription to be dispensed. As of current publicly available information, Daybue is not commercially marketed in India.
However, patients in India can legally access Daybue through the Named Patient Program (NPP) — an import provision that allows patients to receive medicines approved in other countries but not yet marketed in India, under a doctor's prescription and proper regulatory documentation.
Daybue received US FDA approval in March 2023 as the first treatment specifically for Rett syndrome, ensuring full transparency throughout the process.
Daybue can be made available to patients, doctors, and hospitals across major cities in India, including Gurgaon, Delhi, Bangalore, Mumbai, Navi Mumbai, Thane, Hyderabad, Mysore, Kerala, Chennai, Coimbatore, Madurai, Kolkata, Ahmedabad, Surat, Vadodara, Pune, Nagpur, Nashik, Jaipur, Udaipur, Lucknow, Kanpur, Gorakhpur, Chandigarh, Mohali, Faridabad, Noida, Ghaziabad, Kochi, Trivandrum, Kozhikode, Thrissur, Kannur, Mangalore, Bhubaneswar, Patna, Ranchi, Raipur, Guwahati, Visakhapatnam, Vijayawada, Goa, Jammu, Srinagar, Dehradun, Bhopal, Indore, Ludhiana, Amritsar, and others.
Daybue is sourced directly from authorized channels in the country of origin and shipped to India under GDP-compliant, cold-chain logistics to preserve product integrity from dispatch to delivery.
Named Patient Program supports access to Daybue for patients with Rett syndrome across major cities in India, coordinating documentation, sourcing, and delivery with treating specialists.
Patients in Mumbai can access Daybue through NPP with support from treating pediatric neurologists at the city's leading centers.
In Delhi, NPP coordinates with hospitals and specialty neurology clinics to facilitate timely access to Daybue.
Bangalore's pediatric neurology centers work with NPP to support patients requiring Daybue.
Patients in Chennai can access Daybue through NPP, with coordination between treating doctors and the program's regulatory and logistics team.
Hyderabad's pediatric neurology centers support diagnosis and access coordination for Daybue through NPP.
NPP facilitates access to Daybue for patients in Kolkata under the guidance of treating specialists.
Patients in Pune can access Daybue through NPP with prescription-based coordination and cold-chain delivery support.
NPP supports access to Daybue for patients in Ahmedabad, working directly with treating specialists.
Patients in Kochi and across Kerala can access Daybue through NPP's regulated import pathway.
NPP coordinates access to Daybue for patients in Chandigarh and the surrounding region.
Patients in Jaipur can access Daybue through NPP with support from treating specialists.
NPP facilitates access to Daybue for patients in Lucknow and across Uttar Pradesh.
Patients in Bhubaneswar can access Daybue through NPP's coordinated import and delivery process.
NPP supports access to Daybue for patients in Guwahati and across the Northeast region.
NPP also supports access for patients in other Indian cities not listed above — contact the team to check availability and timelines for your location.
Written By: Nitin Goswami, Senior Medical Content Writer
Last Updated: 09 September 2026
Sources: FDA • CDSCO
Medically Reviewed By: Shilpi Banerjee, Registered Pharmacist (M.Pharm)
Last Updated: 09 September 2026
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