A Study Assessing the Safety and Efficacy of Multiple Intravitreal KH902 in Patients With CNV Due to AMD

Neovascular Age-related Macular Degeneration Clinical Trial

— HOPE  

Official title:

An Open Label, Multicenter, Randomized, Uncontrolled Study Assessing the Safety and Efficacy of KH902 in Patients With Choroidal Neovascularization Due to Neovascular Age-related Macular Degeneration(HOPE Study)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01242254
• Other study ID #: KHSWKH902004
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: November 10, 2010
• Last updated: March 25, 2014
• Start date: August 2009
• Est. completion date: February 2011

Study information

• Verified date: July 2011
• 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 assess the efficacy and safety of multiple intravitreal injection of KH902 in patients with CNV due to AMD.

Description:

Due to conclusions of KH902 Ia study:

Doses of single intravitreal injection of a recombinant human VEGF receptor-Fc fusion protein (KH902) in patients with CNV secondary to neovascular AMD are from 0.05 mg to 3.0 mg. The trial shows that KH902 is safe and tolerable, and no DLT, ophthalmia reaction, endophthalmitis, or systemic AE relevant to the drug is reported, and the main AEs are transient ocular tension increase and micro-hemorrhage in injection site. KH902 appears to produce rapid clinical effects on VA, supported by improvements in anatomical features, in patients with neovascular AMD.

HOPE Study is an open label, multi-center, randomized, uncontrolled dose-and interval-ranging phase Ib study designed to assess the efficacy and safety of multiple intravitreal injection of KH902 at variable dosing regimen in patients with CNV due to AMD. Two groups of patients will initially receive intravitreal administration of KH902 following the randomization:

1. Patients in group A will receive monthly intravitreal injections of KH902 for 3 times successively at a dose of 0.5 mg/50 μl/eye;

2. Patients in group B will receive monthly intravitreal injections of KH902 for 3 times successively at a dose of 2.0 mg/50 μl/eye.

Following the initial 12-week fixed-dosing phase of the trial:

Patients in group A and group B will continue to receive monthly intravitreal injections of KH902 with 0.5 mg/50 μl/eye or 2.0 mg/50 μl/eye as same as the doses he/she received during the fixed dosing phase, on an as needed (PRN) dosing schedule, based upon the need for re-treatment in accordance with pre-specified criteria up till week 52.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: February 2011
• Est. primary completion date: March 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 45 Years and older

Eligibility

Inclusion Criteria:

• Signed the Informed Consent Form by patients or legal representative;

• Men and women = 45 years of age;

• Active primary or recurrent lesions with CNV secondary to neovascular AMD;

• Total lesion size = 12 disc areas in either eye;

• BCVA of the study eyes < 69 letters and the BCVA of fellow eyes = 19 letters;

• Clear ocular media and adequate pupil dilation.

Exclusion Criteria:

• CNV lesion secondary to ocular conditions other than neovascular AMD

• History of vitreous hemorrhage, retinal tear, rhegmatogenous retinal detachment or macular hole in the study eye;

• Presence of retinal detachment, retinal pigment epithelial tear, or retinal macular traction in the study eye;

• Anaphylactic disease;

• Uncontrolled glaucoma in either eye;

• Current active ocular inflammation or infection in either eye;

• Previous anti-VEGF drug treatment in the study eye within three months preceding screening, and/or, for the fellow eye, within one month preceding screening;

• Previous ophthalmologic operation or laser therapy in the study eye within three months preceding screening;

• Current non-healing wound, ulcer, fractures, etc;

• Uncontrolled systemic conditions;

• Patients of child-bearing potential do not adopted adequate contraception methods;

• Pregnant or nursing women.

Study Design

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

Related Conditions & MeSH terms

• Choroidal Neovascularization
• Macular Degeneration
• Neovascular Age-related Macular Degeneration
• Wet Macular Degeneration

Intervention

Biological:
• Intravitreal injection of KH902
0.5 mg 2.0 mg once per 4 weeks during fixed dosing phase once as needed during extended treatment phase

Locations

Country	Name	City	State
China	Beijing Tongren Hospital	Beijing	Beijing
China	West China Hospital ,Sichuan University	Chengdu	Sichuan
China	Shanghai First People's Hospital	Shanghai	Shanghai

Sponsors (3)

Lead Sponsor	Collaborator
Chengdu Kanghong Biotech Co.,Ltd.	Fourth Military Medical University, University of Wisconsin, Madison

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The incidence rate of adverse event	To evaluate the safety of multiple intravitreal injection of KH902 of each group.	at 52 week	Yes
Secondary	Change from Baseline in BCVA	To evaluate the efficacy of multiple intravitreal injection of KH902 of each group in the mean change from baseline	Specified timepoints during the screening phase and 52-week treatment period	No