Apnimed’s AD109 Could Be A Wake-Up Call For Sleep Apnea Market

The first of two Phase III trials in obstructive sleep apnea showed Apnimed’s combination pill can offer a therapeutic alternative to entrenched CPAP devices.

WOODEN MAN PUSHING SLEEP APNEA ROCK UPHILL.
Apnimed hopes its combo drug can provide a drug therapy to a wide range of OAS patients • Source: Alamy

Obstructive sleep apnea (OSA) is a therapeutic area with an entrenched therapy – continuous positive air pressure (CPAP) devices – but with the first Phase III data in hand for its combination pill AD109, Apnimed thinks it can enter the market as a monotherapy in OSA or be used in tandem with CPAP or Eli Lilly’s Zepbound (tirzepatide).

Key Takeaways
  • Apnimed reported Phase III success for its sleep apnea combination pill and is awaiting data from a second Phase III study.

The Cambridge, MA-based, privately held biotech expects data from a second Phase III trial in the third quarter and is...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Scrip for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Strategy

Otsuka’s IgAN Data Top Some Vera Results, But To What End?

 
• By 

Otsuka bested Vera on Phase III immunoglobulin A nephropathy data for proteinuria, but analysts wonder if the difference is especially meaningful.

Santen Sees Potential In Myopia Market After Ryjunea Approval

 
• By 

The low-dose atropine eye drop slowed the progression of pediatric myopia by 30%.

Europe’s Drugmakers Lament EU Pharma Package

 
• By 

EFPIA says reforms make the continent less attractive for innovative firms.

Bayer Boosted By Third FDA Approval For Nubeqa

 
• By 

US green light will further expand sales of the prostate cancer blockbuster.

More from Therapy Areas

Lyra Eyes US Filing For LYR-210 After Surprise ENLIGHTEN 2 Win

 

In a turn of fortunes, Lyra Therapeutics has reported positive Phase III results for LYR-210 in chronic rhinosinusitis, boosting hopes for US approval. The company plans to submit an NDA and pursue further trials, but its cash position is precarious.

Ascletis Plans China Submission After Positive Denifanstat Phase III Acne Results

 

Once-daily oral FASN inhibitor denifanstat meets all endpoints in a Chinese Phase III trial for moderate-to-severe acne, paving the way for a regulatory submission in China.

New Regenxbio DMD Data Support Gene Therapy Accelerated Approval

 
• By 

Regenxbio reported functional and biomarker data from an ongoing study of RGX-202, which it hopes to file for approval in Duchenne muscular dystrophy in 2026.