A 12-month, Randomized, Efficacy and Safety Study of 0.5 mg Ranibizumab vs Laser in Chinese Diabetic Macular Edema (DME) Patients

Last updated: January 30, 2019
Sponsor: Novartis Pharmaceuticals
Overall Status: Completed

Phase

3

Condition

Diabetic Retinopathy

Eye Disorders/infections

Vision Loss

Treatment

N/A

Clinical Study ID

NCT02259088
CRFB002D2305
  • Ages > 18
  • All Genders

Study Summary

Study of efficacy and safety of 0.5 mg ranibizumab in Chinese patients with diabetic macular edema (DME)

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  • Male or female Chinese patients ≥ 18 years of age with diabetes mellitus and withHbA1c ≤10.0%

  • Stable medication for diabetes within 3 months prior to Visit 1

  • Visual impairment due to DME with BCVA score between 78 and 39 letters as measured byETDRS-like charts at 4 meters

Exclusion

Key Exclusion Criteria:

  • Stroke or myocardial infarction less than 3 months prior to screening visit

  • Uncontrolled hypertension

  • Active ocular infection or intraocular inflammation in any eye

  • Treatment with any anti-angiogenic drugs within 3 months prior to baseline visit inany eye

  • Active proliferative diabetic retinopathy in study eye

  • Use of other investigational drugs within 30 days and systemic anti-VEGF drugs within 6 months prior to baseline visit

  • Prior laser photocoagulation or intraocular procedure within 3 months prior tobaseline in study eye

  • History of intravitreal corticosteroid treatment in phakic study eye, and in aphakicor pseudophakic within 3 months prior to screening

Study Design

Total Participants: 384
Study Start date:
November 05, 2014
Estimated Completion Date:
January 17, 2017

Study Description

The purpose of this study was to provide efficacy and safety data on 0.5 mg ranibizumab intravitreal injections compared to laser photocoagulation in Chinese patients with visual impairment due to DME. Treatment was driven by achieving vision stabilization.

Connect with a study center

  • Novartis Investigative Site

    Guangzhou, Guangdong 510632
    China

    Site Not Available

  • Novartis Investigative Site

    Shantou, Guangdong 515041
    China

    Site Not Available

  • Novartis Investigative Site

    Harbin, Heilongjiang 150001
    China

    Site Not Available

  • Novartis Investigative Site

    Wuhan, Hubei 430022
    China

    Site Not Available

  • Novartis Investigative Site

    Changsha, Hunan 410011
    China

    Site Not Available

  • Novartis Investigative Site

    Wuxi, Jiangsu
    China

    Site Not Available

  • Novartis Investigative Site

    Nanchang, Jiangxi 330019
    China

    Site Not Available

  • Novartis Investigative Site

    Qingdao, Shandong 2666000
    China

    Site Not Available

  • Novartis Investigative Site

    Xi'an, Shanxi 710032
    China

    Site Not Available

  • Novartis Investigative Site

    Chengdu, Sichuan 610041
    China

    Site Not Available

  • Novartis Investigative Site

    Tianjin, Tianjin 300020
    China

    Site Not Available

  • Novartis Investigative Site

    Hangzhou, Zhejiang 310003
    China

    Site Not Available

  • Novartis Investigative Site

    Wenzhou, Zhejiang 325027
    China

    Site Not Available

  • Novartis Investigative Site

    Beijing, 100034
    China

    Site Not Available

  • Novartis Investigative Site

    Chongqing, 400042
    China

    Site Not Available

  • Novartis Investigative Site

    Shanghai, 200080
    China

    Site Not Available

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