Brolucizumab in the Treatment of Proliferative Diabetic Retinopathy: The CONDOR Randomized Clinical Trial - Scorecard - MDSpire

Brolucizumab in the Treatment of Proliferative Diabetic Retinopathy: The CONDOR Randomized Clinical Trial

  • By

  • Sebastian Wolf

  • Youxin Chen

  • Xiaorong Li

  • Masahiko Shimura

  • Taiji Sakamoto

  • Charles C. Wykoff

  • Andres Emanuelli

  • Hani Salehi-Had

  • Kang Yan

  • Lidija Kovacic

  • Yongsoo Kim

  • June 1, 2026

  • 0 min

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Clinical Scorecard: Efficacy of Brolucizumab for Proliferative Diabetic Retinopathy: Insights from the CONDOR Randomized Clinical Trial

At a Glance

CategoryDetail
ConditionProliferative Diabetic Retinopathy
Key MechanismsPathologic neovascularization driven by upregulation of VEGF due to hyperglycemia and retinal ischemia.
Target PopulationAdults with diabetes type 1 or 2 and proliferative diabetic retinopathy without previous PRP treatment.
Care SettingMulticenter, randomized clinical trial

Key Highlights

  • Brolucizumab is a high-affinity anti-VEGF therapy with a low molecular weight.
  • The CONDOR study is a phase 3 trial comparing brolucizumab to panretinal laser photocoagulation.
  • Participants were randomized 1:1 to receive either brolucizumab or PRP.
  • Brolucizumab treatment involves initial doses every 6 weeks, followed by maintenance every 12 weeks.
  • Key exclusion criteria included center-involved diabetic macular edema and previous PRP.

Guideline-Based Recommendations

Diagnosis

  • Diagnosis of PDR confirmed by standard or widefield color fundus photography and fluorescein angiography.

Management

  • Brolucizumab or PRP as treatment options for PDR.

Monitoring & Follow-up

  • Visual acuity and disease activity should be monitored throughout treatment.

Risks

  • Potential complications of PRP include choroidal effusions and visual field deficits.

Patient & Prescribing Data

Adults aged 18 years or older with diabetes and PDR.

Brolucizumab may offer additional efficacy beyond existing anti-VEGF therapies.

Clinical Best Practices

  • Ensure informed consent is obtained prior to study-related procedures.
  • Follow CONSORT guidelines for reporting clinical trials.
  • Mask site personnel performing visual assessments to maintain study integrity.

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