A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of RO7446603 Administered Alone or in Combination With Aflibercept or Faricimab in Participants With Diabetic Macular Edema

  • Eye Disorder
  • Diabetic Macular Edema
Please note that the recruitment status of the study at your site may differ from the overall study status because some study sites may recruit earlier than others.
Study Status:

Recruiting

This study runs in
Cities
  • Abilene
  • Arecibo
  • Asheville
  • Austin
  • Baltimore
  • Bellaire
  • Clearwater
  • Dallas
  • Durham
  • Encino
  • Fort Myers
  • Germantown
  • Hagerstown
  • Indianapolis
  • Lemont
  • Marietta
  • McAllen
  • Norfolk
  • Phoenix
  • Sacramento
  • San Antonio
  • Springfield
  • The Woodlands
  • Willow Park
Trial Identifier:

NCT06850922 ISRCTN14152148 GR43828

      Show study locations

      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical study see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Study Summary

      This study aims to evaluate the ocular and systemic safety, tolerability and efficacy of RO7446603 in participants with diabetic macular edema (DME). The study consists of 2 segments: Phase I (Parts 1-4) and Phase II (Part 5). Phase I investigated the safety of RO7446603 following a single and multiple intravitreal (IVT) doses as monotherapy or co-administered with IVT aflibercept or IVT faricimab (in separate injections). Phase II will investigate the safety, tolerability, pharmacokinetics (PK) and efficacy of two dose levels of RO7446603 in combination with faricimab, with the two drugs co-mixed and administered as a single IVT injection, compared to faricimab alone. The first participant was enrolled in the Phase I segment on June 22, 2022. Phase I has been completed.

      Genentech, Inc. Sponsor
      Phase 1/Phase 2 Phase
      NCT06850922, GR43828, ISRCTN14152148 Trial Identifier
      RO7446603, Aflibercept, Faricimab Treatments
      Diabetic Macular Edema Condition
      Official Title

      A Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of RO7446603 Administered Alone or in Combination With Aflibercept or Faricimab in Patients With Diabetic Macular Edema

      Eligibility Criteria

      gender
      All Gender
      age
      ≥18 Years Age
      healthy-volunteers
      No Healthy Volunteers
      Inclusion Criteria
      • Documented diagnosis of diabetes mellitus (DM) (Type 1 or Type 2) with glycated hemoglobin (HbA1c) < 12%
      • Macular thickening secondary to DME involving the center of the fovea > 325 microns
      • Decreased VA attributable primarily to DME between 25 and 73 ETDRS letters
      Exclusion Criteria
      • Currently untreated DM or previously untreated participants who initiated oral anti-diabetic medication or insulin within 90 days prior to Day 1
      • Uncontrolled blood pressure (BP)
      • Pregnancy or breastfeeding, or intention to become pregnant during the study
      • For Parts 1-4: IVT anti-VEGF treatment within 90 days prior to Day 1; For Part 5: IVT anti-VEGF treatment within 120 days prior to Day 1 or IVT anti-VEGF treatment prior to Day 1 for treatment naïve participants
      • Treatment with SUSVIMOTM (ranibizumab injection) prior to Day 1
      • Any IVT or periocular (sub-tenons) corticosteroid treatment within 6 months prior to Day 1
      • Any current or history of ocular disease other than DME that may confound assessment of the macula or affect central vision
      • Proliferative diabetic retinopathy (PDR) in the study eye
      • Active or history of uveitis, vitritis (grade trace or above), and/or scleritis in either eye Other protocol-specified inclusion/exclusion criteria may apply

      For the latest version of this information please go to www.forpatients.roche.com

       

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