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

Phase
Phase 1/Phase 2
Recruitment status
Participants
Lead sponsor
Genentech, Inc.
Start date
Number of sites

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.
Acronym
Short title
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
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

Registry reports results
Listing at source
Recruitment status
Phase
Phase 1/Phase 2
Study type
Interventional

Completion date
First posted
Registry last updated
Primary completion date
Start date

Actual participants
Participants
Participant count basis
Protocol amendments
Number of sites

Data monitoring committee
Registry sponsor category
Lead sponsor
Genentech, Inc.
Source registry
ClinicalTrials.gov

Registry ID
ClinicalTrials.gov ID
Registry record
Open registry record

Allocation
Randomised
Model
Sequential
Purpose
Treatment
Masking
Quadruple masking
Masking description
The Phase 1 segment of this study was open-label and participants were randomized in Part 4. The Phase 2 segment will be a randomized, double-blinded study.
Masked roles
Participants, Care providers, Investigators, Outcome assessors
Sources for study design

  1. Parts 1-5: Percentage of Participants With Adverse Events (AEs)

    Timeframe: From study start through end of study (Up to approximately 58 months)

  2. Parts 1-5: Percentage of Participants With Ocular AEs

    Timeframe: From study start through end of study (Up to approximately 58 months)

  3. Part 1: Change in Best Corrected Visual Acuity (BCVA) Over Time

    Timeframe: From Baseline up to Week 16

    BCVA will be measured via Early Treatment Diabetic Retinopathy Study (ETDRS) chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified visual acuity (VA) examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  4. Parts 2-4: Change in BCVA Over Time

    Timeframe: From Baseline up to Week 28

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  5. Part 5: Change From Baseline in BCVA Averaged Over Weeks 52 and 56

    Timeframe: From Baseline up to Week 56

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  1. Part 5: Proportion of Participants Gaining ≥ 15 Letters in BCVA From Baseline Averaged Over Weeks 52 and 56

    Timeframe: From Baseline up to Week 56

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  2. Part 5: Percentage of Participants Gaining ≥ 15, ≥ 10, ≥ 5, or ≥ 0 Letters in BCVA From Baseline Over Time

    Timeframe: From Baseline up to Week 56

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  3. Part 5: Percentage of Participants Avoiding a Loss of ≥ 15, ≥ 10, ≥ 5, or ≥ 0 Letters in BCVA From Baseline Over Time

    Timeframe: From Baseline up to Week 56

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  4. Part 5: Change From Baseline in BCVA Score Over Time

    Timeframe: From Baseline up to Week 56

    BCVA will be measured via ETDRS chart at a starting distance of 4 meters using a set of three precision VisionTM or lighthouse distance acuity charts (modified ETDRS Charts 1, 2, and R) prior to dilating eyes by a trained and certified VA examiner. The range of EDTRS is 0 to 100 letters. Higher scores indicate improvement in VA.

  5. Parts 1-4: Serum Concentration of RO7446603 Total Fab

    Timeframe: Part 1: From Baseline up to Week 16; Parts 2-4: From Baseline up to Week 28

  6. Parts 1-5: Aqueous Humor Concentration of RO7446603 Measured as Total Fab

    Timeframe: From study start through end of study (Up to approximately 58 months)

  7. Parts 1-5: Number of Participants With Serum Treatment-emergent Anti-drug Antibody (ADA) Formation to RO7446603

    Timeframe: From study start through end of study (Up to approximately 58 months)

Sources for outcomes

Sex
All
Age groups
Adults, Older adults
Minimum age
18 Years
Healthy volunteers
No

  • 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

  • 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
Sources for eligibility

  • Arizona Retina and Vitreous ConsultantsPhoenix, United States
  • Associated Retinal Consultants PCPhoenix, United States
  • Retinal Research Institute, LLCPhoenix, United States
  • Retina Partners of Northwest Arkansas, PLLCSpringdale, United States
  • Retinal Diagnostic CenterCampbell, United States
  • Retina Consultants of Orange CountyFullerton, United States
  • Retinal Consultants Medical GroupModesto, United States
  • Northern California Retina-Vitreous AssociatesMountain View, United States
  • Retinal Consultants Medical GroupSacramento, United States
  • University of California San FranciscoSan Francisco, United States
  • Macula Retina Vitreous Research InstituteTorrance, United States
  • Bay Area Retina Associates;Study DepartmentWalnut Creek, United States
  • University of Colorado - Eye Center - PPDSAurora, United States
  • Retina Consultants of Southern Colorado PCColorado Springs, United States
  • Retina Specialists of ColoradoDenver, United States
  • Advanced Vision Research InstituteLongmont, United States
  • Retina Group of New EnglandWaterford, United States
  • National Ophthalmic Research InstituteFort Myers, United States
  • Florida Retina InstituteJacksonville, United States
  • Retina Associates of Florida;Retina Associates of FloridaTampa, United States
  • Southeast Retina CenterAugusta, United States
  • Georgia Retina PCMarietta, United States
  • Retina Consultants of Hawaii‘Aiea, United States
  • Illinois Eye and Ear InfirmaryChicago, United States
  • University Retina and Macula Associates, PCOak Forest, United States

And 52 more, listed on the interactive page.

Sources for sites

Other registry identifiers

  • ISRCTN14152148
Sources for references

Related records

Drugs (2)

Lead sponsors (1)

Conditions (1)

Targets (3)