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By physician referral or invitation only

GBT021601-021

To evaluate the safety, tolerability, and efficacy of GBT021601 in adult participants with SCD to determine an optimal dose.

Age & Gender

  • 18 years ~ 65 years
  • Male, Female, Gender Inclusive

Contact the Team

Location

Thank you for your interest, but this study is recruiting by invitation only.

North Carolina (Statewide)

Additional Study Information

Principal Investigator

Jane Little
Medicine-Hematology

Study Type

Clinical or Medical
Interventional

Study Topics

Blood Conditions
Rare Diseases

IRB Number

23-0416

ClinicalTrials.gov

NCT05431088

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