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L'AYP-101 d'AMI Pharm montre des résultats prometteurs lors d'un essai de phase 2, ce qui laisse présager une avancée décisive dans la réduction non chirurgicale de la graisse
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AMI Pharm

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AMI Pharm

Sep 01, 2025, 03:00 ET

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  • L'« AYP-101 » d'AMI Pharm est en passe de devenir un nouveau leader de la réduction non chirurgicale de la graisse grâce au succès de l'essai de phase 2
  • Les résultats cliniques de l'« AYP-101 », une solution non chirurgicale prometteuse, sont publiés dans Clinical Therapeutics
  • L'« AYP-101 » démontre une sécurité et une efficacité supérieures et devrait changer le paradigme de la réduction de la graisse sous-mentonnière.

SÉOUL, Corée du Sud, 1er septembre 2025 /PRNewswire/ -- Le nouveau médicament injectable d'AMI Pharm, l'AYP-101, a montré des résultats prometteurs lors d'un essai de phase 2 pour réduire la graisse sous-mentonnière, communément appelée double menton. Les résultats de l'étude ont été récemment publiés dans Clinical Therapeutics, une revue de premier plan pour le développement de médicaments et de traitements. Cette publication marque une étape importante pour l'AYP-101 et souligne son potentiel en tant que traitement non chirurgical sûr et efficace. L'étude a évalué l'efficacité et la sécurité de l'AYP-101 à deux concentrations différentes. Les résultats ont montré que la concentration de 25 mg/mL, administrée toutes les deux semaines pendant six séances, conduisait à des réductions statistiquement significatives et cliniquement significatives de la graisse sous-mentonnière.

Une efficacité et une sécurité démontrées

L'étude de phase 2 a recruté 96 participants et a démontré de solides résultats. Quatre semaines après le dernier traitement, 69,70 % des participants du groupe traité à 25 mg/mL ont obtenu une amélioration d'au moins un degré sur les échelles d'évaluation de la graisse sous-mentonnière rapportée tant par l'évaluateur que par le sujet (ER-SMFRS et SR-SMFRS). Il s'agit d'une amélioration statistiquement significative par rapport au taux de réponse de 22,58 % dans le groupe placebo. Les données de l'essai ont également mis en évidence le profil de sécurité et de tolérance favorable de l'AYP-101. Le médicament est conçu de manière unique pour éliminer la graisse par un processus appelé apoptose tout en limitant les dommages aux tissus environnants. L'étude a montré que l'AYP-101 nécessitait moins de points d'injection et produisait une incidence plus faible de gonflement et de paresthésie après l'injection que ce qui est généralement rapporté pour l'acide désoxycholique (DCA).

Un leader sur le marché de l'esthétique en pleine croissance

Face à l'augmentation de la demande mondiale de réduction non chirurgicale de la graisse, AMI Pharm poursuit le développement de l'AYP-101. Selon Ki-Taek Lee, PDG d'AMI Pharm, « La publication de la phase 2 réaffirme notre force en matière de R&D et démontre le potentiel significatif de l'AYP-101 sur le marché de la réduction de la graisse localisée ». L'étude de phase 3 de l'AYP-101 est en cours d'accélération, l'objectif étant qu'elle soit terminée fin 2025. AMI Pharm développe aussi activement des collaborations internationales pour mettre au point des médicaments injectables de nouvelle génération pour la réduction de la graisse localisée. Cette dernière publication fait suite aux résultats positifs de l'étude de phase 1 de l'AYP-101 en 2024, confirmant ainsi sa reconnaissance internationale.

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