Pratteln, Switzerland, 29 August, 2025 - Santhera Pharmaceuticals (SIX: SANN) announces the signing of an exclusive agreement with Ikris Pharma Network (Ikris) to manage the distribution of AGAMREE® (vamorolone) in India, for the treatment of Duchenne muscular dystrophy (DMD) in patients four years of age and older.
The agreement between Santhera and Ikris has a 5-year term and Santhera will receive a percentage of net sales, in line with previous distribution agreements. Sales are expected to begin in Q4 2025 on a named patient basis.
Today's agreement follows recent distribution deals secured in Turkey and a range of Gulf Cooperation Council countries. Santhera continues to press ahead with the global rollout of AGAMREE.
Dario Eklund, Chief Executive Officer of Santhera, said: "We are pleased to partner with Ikris Pharma Network in India, which is part of our wider strategy to increase global access to AGAMREE for patients with DMD. Ikris has been actively working in the area of DMD and their expertise and dedication to ensuring rare disease drugs reach patients makes them an ideal partner in the region."
Praveen Sikri, Founder & CEO of Ikris Pharma Networksaid: "This collaboration with Santhera aligns with our focus of addressing unmet medical needs in the rare disease community. We look forward to leveraging our distribution network to help DMD patients in India access this life-changing treatment."
About AGAMREE® (vamorolone)
AGAMREE is a novel drug with a mode of action based on binding to the same receptor as glucocorticoids but modifying its downstream activity. Moreover, it is not a substrate for the 11-ß-hydroxysteroid dehydrogenase (11ß-HSD) enzymes that may be responsible for local drug amplification and corticosteroid-associated toxicity in local tissues [1-4]. This mechanism has shown the potential to 'dissociate' efficacy from steroid safety concerns and therefore AGAMREE is positioned as a dissociative anti-inflammatory drug and an alternative to existing corticosteroids, the current standard of care in children and adolescent patients with DMD [1-4].
In the pivotal VISION-DMD study, AGAMREE met the primary endpoint Time to Stand (TTSTAND) velocity versus placebo (p=0.002) at 24 weeks of treatment and showed a good safety and tolerability profile [1, 4]. The most commonly reported side effects were cushingoid features, vomiting, weight increase and irritability. Side effects were generally of mild to moderate severity.
Currently available data show that AGAMREE, unlike corticosteroids, has no restriction of growth [5] and no negative effects on bone metabolism as demonstrated by normal bone formation and bone resorption serum markers [6].
? This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.
References:
[1] Dang UJ et al..
[2] Guglieri M et al.
[3] Liu X et al.
[6] Hasham et al., MDA 2022 Poster presentation. Link.
About Santhera
Santhera Pharmaceuticals.
AGAMREE® is a trademark of Santhera Pharmaceuticals.
About Ikris Pharma Network
Ikris Pharma Network is India's biggest named patient supply company, specializing in providing access to rare disease medications. With established expertise in logistics, regulatory compliance, and patient access programs, Ikris has supported physicians and patients in obtaining therapies that are not locally available. The company has been actively working in the area of Duchenne muscular dystrophy (DMD), providing assistance to patients and healthcare professionals in India.
Partnership Impact:
Through its authorization with Santhera Pharmaceuticals, Ikris Pharma Network will facilitate access to AGAMREE® (vamorolone) for eligible patients with Duchenne Muscular Dystrophy in India. The collaboration aims to provide a regulatory-compliant pathway for access and strengthen existing efforts in patient support and disease awareness in the country.
Duchenne Muscular Dystrophy (DMD):
DMD is a rare genetic disorder caused by mutations in the dystrophin gene, leading to progressive muscle weakness that usually begins in early childhood. Most patients lose ambulation in adolescence. While there is no cure, available treatments such as corticosteroids and supportive care can help manage symptoms. Expanding access to therapies like AGAMREE is intended to support the ongoing care of patients and families living with DMD in India.
For further information please contact:
Santhera
Catherine Isted, Chief Financial Officer: IR@santhera.com
ICR Healthcare: Santhera@icrhealthcare.com
Ikris Pharma Network
Praveen Sikri, Chief Executive Officer: info@ikrispharmanetwork.com
Bharat Sikri, Global Project Manager: Raredisease@ikrispharmanetwork.com
Disclaimer / Forward-looking statements
This communication does not constitute an offer or invitation to subscribe for or purchase any securities of Santhera Pharmaceuticals Holding AG. This publication may contain certain forward-looking statements concerning the Company and its business. Such statements involve certain risks, uncertainties and other factors which could cause the actual results, financial condition, performance or achievements of the Company to be materially different from those expressed or implied by such statements. Readers should therefore not place undue reliance on these statements, particularly not in connection with any contract or investment decision. The Company disclaims any obligation to update these forward-looking statements.
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Attachment
- 250829 Santhera India Ikris Distribution Agreement -FINAL (https://ml-eu.globenewswire.com/Resource/Download/dac39f31-694c-414b-8d1a-bf39e45067bb)
