New Zealand researchers are set to conduct ‘Reclaim’, the world’s first trial of Kriya-586, a one-time treatment with the potential to “turn off” thyroid eye disease (TED).
US company Kriya Therapeutics describes its product as an adeno-associated virus gene therapy that drives durable expression of a monoclonal antibody that blocks insulin-like growth factor 1 receptors (IGF-1R). “This decreases pro-inflammatory thyrotropin receptor autoantibody signalling, which may lead to reductions in proptosis and diplopia. IGF-1R blockade has been established as a clinically validated mechanism of action [in patients with TED],” the company said.
That clinical validation comes courtesy of teprotumumab (Tepezza), an FDA-approved treatment for active, moderate-to-severe TED. Administered via intravenous infusion every three weeks for a total of eight doses, it reduces proptosis and inflammation by targeting orbital fibroblasts, according to the European Medicines Agency.
Kriya Therapeutics recognised that local production of teprotumumab might be effective in controlling TED, explained Christchurch’s Dr Rebecca Stack, one of the Reclaim study co-investigators. “[It used the theory that] delivering genetic material to the affected tissue by peribulbar injection will lead to local production of teprotumumab for the life of the orbital fibroblasts… a one-off injection, turning off the disease and curing the patient.”
While teprotumumab has been available in Australia since June 2025, it is not yet available in New Zealand. However, a July 2025 meeting of Medsafe’s Medicines Classification Committee recommended that it be added to the New Zealand Medicines Schedule as a prescription medicine.








