Biomarin Withdraws Voxzogo Reimbursement Application in the Netherlands

By HEOR Staff Writer

March 16, 2026

Voxzogo reimbursement Netherlands hangs in limbo after Biomarin’s decision on March 12, 2026, to withdraw its application, leaving children with achondroplasia without access despite parental pleas. Zorginstituut Nederland voices deep regret over the move, citing petitions like one with 34,615 signatures by September 23, 2025, and urges the manufacturer to reverse course.

Parental Pleas Ignored by Biomarin

Biomarin has refused to pursue Voxzogo reimbursement Netherlands, despite urgent requests from parents of children with achondroplasia, a form of dwarfism. Zorginstituut organized special meetings with parents, patients, healthcare professionals, and Biomarin to discuss conditional reimbursement, highlighting the agency’s commitment amid the manufacturer’s inaction.

Zorginstituut Nederland proactively consulted Biomarin multiple times after Voxzogo’s 2021 EMA approval, an rare initiative since no reimbursement application followed. These steps aimed to aid a small patient group, while emphasizing the manufacturer’s responsibility.

Fallout for Patients and Market Access

Biomarin’s stance denies Dutch children a globally available therapy, fueling frustration and Zorginstituut’s reversal call. It highlights orphan drug pricing tensions, potentially deterring submissions in cost-conscious markets like the Netherlands. This stresses discussions for sustainable Voxzogo reimbursement in the Netherlands.

Reference url

Recent Posts

Expanding Access to Hormonal IUDs in South Africa through Generic Innovation

By HEOR Staff Writer

April 27, 2026

The launch of AVIBELA marks a significant milestone for hormonal IUD South Africa, introducing the country’s first generic levonorgestrel 52 mg intrauterine device. Developed by Medicines360 and commercialized in partnership with Pharma Dynamics, AVIBELA is more than 99% effective at preventing p...
Regulatory Divergence in PSMA Targeted Therapy: Implications for European Market Access
Novartis withdrew its European Medicines Agency (EMA) application to expand the indication for Pluvicto® (lutetium (177Lu) vipivotide tetraxetan). The company sought to include adult patients with PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) who have not yet received chem...
PIONEER TEENS Trial Reveals Oral Semaglutide Diabetes Breakthrough for Pediatric Patients

By João L. Carapinha

April 24, 2026

Important results from the PIONEER TEENS phase 3a trial! Oral semaglutide diabetes therapy delivered statistically superior glycemic control compared with placebo in children and adolescents aged 10–17 years with type 2 diabetes. The trial met its primary endpoint with a 0.83% greater reduction i...