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Taking people in United StatesPhase 2

A Long-term Extension Study of ORX750 in Participants With Narcolepsy and Idiopathic Hypersomnia

Key facts

Where
Abington, Atlanta, Auburn, Austin, Cincinnati, Denver, Dublin, El Paso, Henderson, Huntersville, Miami, North Charleston, Orlando, Santa Ana, Sterling Heights, Willow Grove, and Winter Park, United StatesSee the 19 sites
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07096674, who can take part

Where in United States

  • Abington, PennsylvaniaAbington, United StatesContact: Orexin Centessa Program LeadTaking people
  • Atlanta, GeorgiaAtlanta, United StatesContact: Orexin Centessa Program LeadTaking people
  • Stockbridge, GAAtlanta, United StatesContact: Orexin Centessa Program LeadTaking people
  • Auburn, AlabamaAuburn, United StatesContact: Orexin Centessa Program LeadTaking people
  • Austin, TexasAustin, United StatesContact: Orexin Centessa Program LeadTaking people
  • Cincinnati, OhioCincinnati, United StatesContact: Orexin Centessa Program LeadTaking people
  • Denver, North CarolinaDenver, United StatesContact: Orexin Centessa Program LeadTaking people
  • DublinDublin, United StatesContact: Orexin Centessa Program LeadTaking people
  • El Paso, TexasEl Paso, United StatesContact: Orexin Centessa Program LeadTaking people
  • Hendersen, NavadaHenderson, United StatesContact: Orexin Centessa Program LeadTaking people
  • Henderson, NevadaHenderson, United StatesContact: Orexin Centessa Program LeadTaking people
  • Huntersville, North CarolinaHuntersville, United StatesContact: Orexin Centessa Program LeadTaking people
  • Miami, FloridaMiami, United StatesContact: Orexin Centessa Program LeadTaking people
  • North Charleston, South CarolinaNorth Charleston, United StatesContact: Orexin Centessa Program LeadTaking people
  • Orlando, FloridaOrlando, United StatesContact: Orexin Centessa Program LeadTaking people
  • Santa Ana, CaliforniaSanta Ana, United StatesContact: Orexin Centessa Program LeadTaking people
  • Sterling Heights, MichiganSterling Heights, United StatesContact: Orexin Centessa Program LeadTaking people
  • Willow Grove, PennsylvaniaWillow Grove, United StatesContact: Orexin Centessa Program LeadTaking people
  • Winter Park, FLWinter Park, United StatesContact: Orexin Centessa Program LeadTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Centessa Pharmaceuticals (UK) Limited
Trial code
NCT07096674EU 2025-522987-34-00
Record updated
16 April 2026
Original description
This study is a long-term extension (LTE) of the parent Study ORX750 0201, and will provide long-term open-label safety, tolerability, and efficacy of ORX750 in participants with narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia (IH).Read full original descriptionShow less

A Phase 2, Long-term Extension Study of the Safety and Efficacy of ORX750 in Participants With Narcolepsy and Idiopathic Hypersomnia Who Completed a Sponsored ORX750 Clinical Trial

This study is a long-term extension (LTE) of the parent Study ORX750 0201, and will provide long-term open-label safety, tolerability, and efficacy of ORX750 in participants with narcolepsy type 1 (NT1), narcolepsy type 2 (NT2), and idiopathic hypersomnia (IH).

Inclusion: Diagnosis of narcolepsy (NT1 or NT2) or IH who was eligible for and completed the full treatment period in the eligible parent study ORX750-0201 (CRYSTAL-1); Is willing and able to adhere to additional protocol requirements.

Exclusion: Unable to refrain from excluded medications, including those used for treatment of narcolepsy or idiopathic hypersomnia; Development of any new disease/disorder that in the opinion of the investigator would make the participant unable to continue the study.

ClinicalTrials.gov NCT07096674 · EU CTIS 2025-522987-34-00