Friday, October 2, 2026

Aroxybutynin and atomoxetine (AD109) for obstructive sleep apnea: a randomized phase 3 trial (SynAIRgy) | American Journal of Respiratory and Critical Care Medicine | Oxford Academic


At a Glance Commentary.

Atomoxetine

Aroxybutynin





Scientific Knowledge on the Subject: AD109 (aroxybutynin 2.5 mg/atomoxetine 75 mg), an investigational, first-in-class, once-daily oral tablet, is designed to target the neuromuscular dysfunction underlying obstructive sleep apnea (OSA) by increasing upper airway muscle tone during sleep. In the phase 2b MARIPOSA trial, AD109 demonstrated significant improvement in the apnea–hypopnea index (AHI) in adults with mild-to-severe OSA over 4 weeks. An earlier phase 2 study suggested that AD109 may reduce AHI from the first dose. AD109 efficacy/safety beyond 4 weeks remain unknown.

What This Study Adds to the Field: SynAIRgy, a part of one of the largest clinical development efforts conducted for an OSA pharmacotherapy, is one of 2 phase 3 registrational trials evaluating the efficacy/safety of AD109. SynAIRgy is a randomized, double-blind, placebo-controlled, parallel-arm trial conducted in 646 participants with mild-to-severe OSA who were intolerant to or refused positive airway pressure therapy. SynAIRgy demonstrated significant improvements in airway obstruction and oxygenation across mild-to-severe OSA participants, supporting the potential for AD109 to be a new oral treatment option for patients with mild-to-severe OSA. Given existing OSA therapy limitations, AD109 may fill a large unmet medical need in providing patients with a pharmacologic therapy targeting the neuromuscular dysfunction underlying OSA pathogenesis.

https://academic.oup.com/ajrccm/advance-article/doi/10.1093/ajrccm/aamag215/8680221?login=false
https://en.wikipedia.org/wiki/Atomoxetine
https://drugs.ncats.io/substance/5BRQ29UUB7

Thursday, October 1, 2026

Teriparatide + Zoledronic Acid Does Not Reduce Fracture Risk in Osteogenesis Imperfecta

In continuation of my update on Teriparatide and  Zoledronic Acid



Among adults with osteogenesis imperfecta, teriparatide plus zoledronic acid does not reduce fracture risk compared with standard care, according to a study published online May 14 in the Journal of the American Medical Association.

Jannie Dahl Hald, Ph.D., from Aarhus University Hospital in Denmark, and colleagues examined whether the parathyroid hormone analogue teriparatide followed by zoledronic acid reduces the risk for fractures in adults with osteogenesis imperfecta in a multicenter randomized clinical trial. Participants were randomly assigned to receive 20 μg of teriparatide daily by subcutaneous injection for two years, followed by 5 mg zoledronic acid infusion (176 participants), or to standard care, in which bisphosphonates and other bone-targeted medicines could be used (174 participants).

Most of the participants had type I osteogenesis imperfecta caused by pathogenic variants in the type 1 collagen genes. The researchers found that 36.9 and 36.4 percent of patients in the teriparatide plus zoledronic acid group and the standard care group, respectively, had incident fractures. There was significantly more of an increase in lumbar spine and total hip bone mineral density with teriparatide plus zoledronic acid than standard care. Teriparatide plus zoledronic acid was favored in several quality-of-life measures. The groups reported similar adverse events.

"We have been using drugs to increase bone density for decades in the hope that they might prevent fractures but the TOPaZ trial clearly shows that these medicines simply do not work," lead author Stuart Ralston, M.D., from the University of Edinburgh Institute of Genetics and Cancer in the United Kingdom, said in a statement.

Ref : https://jamanetwork.com/journals/jama/fullarticle/2849063
https://en.wikipedia.org/wiki/Zoledronic_acid
https://en.wikipedia.org/wiki/Teriparatide

Teriparatide + Zoledronic Acid Does Not Reduce Fracture Risk in Osteogenesis Imperfecta - Drugs.com MedNews