UCB offers helpful resources for your patients with early-onset TK2d.
ONWARD® is a single point of entry for patients to experience personalized support while taking KYGEVVI
Prescribed patients and their caregivers will receive:
Personalized support from a dedicated Care Coordinator* throughout the treatment journey
Coordination between PANTHERx Rare, the exclusive specialty pharmacy for KYGEVVI, and ONWARD’s case management team throughout the insurance approval process
Help with reviewing insurance coverage and potential financial assistance options
Preparation and administration support from PANTHERx Rare
Tools and resources to get started and ongoing treatment support
Start patients prescribed KYGEVVI with ONWARD for comprehensive support
Complete the ONWARD Start Form with your patient during their next visit, or initiate your patient's enrollment via an e-Start Form.
Fax the completed form to: 1‑833‑FAX‑UCB‑1 1-833-FAX-UCB-1 (1‑833‑329‑8221).
*ONWARD Care Coordinators do not provide medical advice and will refer patients to their healthcare professional for any questions related to their treatment plan.
The Music Box: An early-onset TK2d story
Every person with early-onset TK2d experiences their own unique journey to diagnosis and treatment. Watch the journey of a father and his son as they experience the onset of symptoms, search for a diagnosis, and ultimately receive treatment.
Individual results may vary.
Download these resources to help with KYGEVVI access.
Download these resources for information about KYGEVVI.
Download these helpful resources for patients who are prescribed KYGEVVI.
Connect with the mitochondrial disease community
Additional resources from advocacy groups are available to you and your patients.
MitoAction aims to improve the quality of life of people living with mitochondrial diseases through support, education, and outreach.
Mitochondrial Care Network (MCN) creates and implements best practices in mitochondrial medicine.
Muscular Dystrophy Association (MDA) provides support and resources for people living with neuromuscular diseases like TK2d.
The United Mitochondrial Disease Foundation (UMDF) provides resources, patient support, a database of experts, and more.