Safety and Efficacy by Multiple Injection of KH902 in Patients With Diabetic Macular Edema (DME)

Diabetic Macular Edema Clinical Trial

— Frontier-1  

Official title:

An Open-label, Randomized, Uncontrolled, Preliminary Clinical Study to Evaluate the Safety and Efficacy of KH902 Following Multiple Intravitreal Injection in Patients With Diabetic Macular Edema

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01324869
• Other study ID #: KHSWKH902002
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: March 15, 2011
• Last updated: February 28, 2013
• Start date: April 2010
• Est. completion date: October 2012

Study information

• Verified date: February 2013
• Source: Chengdu Kanghong Biotech Co.,Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This study is designed to access the safety and efficacy of multiple injections of KH902 in patients with Diabetic Macular Edema (DME).

Description:

With improvement of our living standard, patients who suffered from Diabetes become more and more. As the investigators know, Diabetes can induce many ocular diseases leading to vision loss. And according to observations, DME is diagnosed as one main cause of vision loss in the patients with Diabetes.

As the results of many studies conducted previously, anti-VEGF drugs and anti-VEGF treatments show its effect and safety not only in treating AMD, but also in patients with DME. The new drug Recombinant Human VEGF Receptor-Fc Fusion Protein (KH902) is a gene fusion protein. The previous clinical trials of KH902 show that KH902 is effective and safe in inhibiting the growth, migration, pullulation of vascular endothelial cells and neovascularization induced by VEGF. Due to these positive results, the investigators prepare to conduct a clinical trial to assess the safety and efficacy with intravitreal injection of KH902 in patients with DME.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: October 2012
• Est. primary completion date: February 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Signed the Informed Consent Form and willing to comply with study procedures;

• 18 years old ? either gender ? 75 years old;

• Confirmed diagnosed with Type 1 diabetes or Type 2 diabetes based on the diabetes diagnosis criteria;

• Clinically significant DME:

• Hard exudation within 500µm of the central foveal diameter accompanied with contiguous retina thickening;

• The edema locates within 500µm of the central foveal diameter;

• Retina thickening field > 1DD and within the 1DD central fovea.

• BCVA score of the study eyes between 78 and 19 letters, inclusively, and the BCVA score of fellow eyes = 24 letters;

• Previous treatment of antidiabetic drugs within three months preceding the screening, and blood-glucose concentration is predicted to be unchanged and stable during the whole study.

Exclusion Criteria:

• Uncontrolled glaucoma in either eye;

• Currently active ocular inflammation or infection in either eye;

• Macular edema in the study eye was caused by other diseases rather than diabetes;

• Company with any other ocular conditions failing to prevent vision loss despite improving the macular edema;

• Any other ocular diseases which may cause macular edema or vision alteration during study phase;

• Retinal macular traction or macular epiretinal membrane in study eye;

• Refractive error equate or exceed 8 diopters of myopia in study eye

• Whole or regional retinal laser photocoagulation has been applied in study eye within 6 months preceding the screening;

• Previous anti-VEGF drug treatment in study eye;

• Intraocular or periocular injection of steroid drug within 6 months preceding the screening;

• Previous ophthalmologic operation within 3 months preceding the screening and/or planning to receive an ophthalmologic operation during the study.

• There is any potential for the study eye to receive the panretinal laser photocoagulation treatment during the study;

• Previous vitrectomy in study eye.

• Uncontrolled diabetes;

• Hypertensive patients with poorly controlled blood pressure;

• Uncontrolled systemic infectious diseases;

• Systemic immune diseases;

• History of allergy;

• Any uncontrolled clinical disorders;

• Pregnant or nursing women;

• Adopt one or more adequate contraception methods.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetic Macular Edema
• Edema
• Macular Edema

Intervention

Biological:
• KH902
Intravitreal injection of 0.5mg/eye/time KH902

Locations

Country	Name	City	State
China	Shanghai First People's Hospital	Shanghai

Sponsors (3)

Lead Sponsor	Collaborator
Chengdu Kanghong Biotech Co.,Ltd.	Teaching and Research Office of Health Statistics, Fourth Military Medical University, University of Wisconsin, Madison

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence rate of adverse event	To evaluate the safety of multiple intravitreal injection of KH902 to treat DME.	up to 12 months	Yes
Secondary	Change from Baseline in BCVA	To evaluate the efficacy of multiple intravitreal injection of KH902 of each group.	at the end of month 3 and the end of month 12	No