A Study of IBI311 in Subjects With Active Thyroid Eye Disease

Thyroid Eye Disease Clinical Trial

Official title:

A Multicenter, Randomized, Double-masked, Placebo-controlled Phase II/III Study Evaluating the Efficacy and Safety of IBI311 in Subjects With Active Thyroid Eye Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05795621
• Other study ID #: CIBI311A201
• Status: Completed
• Phase: Phase 2/Phase 3
• Start date: February 14, 2023
• Est. completion date: December 20, 2023

Study information

• Verified date: February 2024
• Source: Innovent Biologics (Suzhou) Co. Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter, randomized, double-masked, placebo-controlled Phase II/III study in subjects with active thyroid eye disease. Approximately 114 subjects meeting study eligibility criteria will be randomly assigned to IBI311 or placebo on day 1 (D1) in a 2:1 ratio stratified by smoking status

Recruitment information / eligibility

• Status: Completed
• Enrollment: 115
• Est. completion date: December 20, 2023
• Est. primary completion date: December 20, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Key Inclusion Criteria:

1. Written informed consent.

2. Male or female subject between the ages of 18 and 80 years, inclusive, at Screening.

3. Weight between 45 and 100 kg (inclusive).

4. Clinical diagnosis of Graves' disease associated with active TED with a CAS = 3 for at least one eye at Screening and Baseline.

5. Moderate-severe active TED (not sight-threatening but has an appreciable impact on daily life), usually associated with at least two of the following: lid retraction =2 mm, moderate or severe soft tissue involvement, exophthalmos = 3 mm above normal for race and gender, and/or inconstant or constant diplopia.

6. Female Subjects should be fertile women who are sterile or have a negative blood pregnancy test during the screening period and who agree to take contraceptive measures within 120 days from the screening period to the last medication; Male subjects should agree to use contraception from the screening period to 120 days after the last dose.

Key Exclusion Criteria:

Subjects will be ineligible for study participation if they meet any of the following criteria:

1. At the time of screening, according to the subject's chief complaint or medical record, the time of first symptoms of active thyroid eye disease appeared in > 270 days;

2. Optimal corrected vision loss due to optic neuropathy, defined as two lines of vision loss due to optic neuropathy within the past 180 days, new visual field defects, or color vision impairment secondary to optic nerve involvement;

3. Corneal ulcers with no relief after treatment were determined by the investigator;

4. Baseline CAS decreased by more than 2 points compared with screening;

5. At any time prior to baseline or during the study period planned to receive orbital radiation therapy or TED specific surgery, including orbital decompression, strabismus surgery, and eyelid retraction correction;

6. Poor thyroid function control was defined as free triiodothyronine (FT3) or free tetriodothyronine (FT4) deviated more than 50% from the normal reference range of the local research center laboratory during screening;

Related Conditions & MeSH terms

• Eye Diseases
• Graves Ophthalmopathy
• Thyroid Diseases
• Thyroid Eye Disease

Intervention

Biological:
• IBI311
10 mg/kg on Day 1 followed by 20 mg/kg q3W for the remaining 7 infusions for phase II/III.
• placebo
4 does of placebo for phase II; 8 does of placebo for phase III.

Locations

Country	Name	City	State
China	Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Innovent Biologics (Suzhou) Co. Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The proptosis responder rate of the study eye (defined as percentage of subjects with a = 2mm reduction from Baseline in proptosis in the study eye, without deterioration [= 2 mm increase] of proptosis in the non-study eye).	proptosis assessment: amount of protrusion of the eye from the orbital rim measured by Hertel exophthalmometer	Week 12 for phase II, Week 24 for phase III
Secondary	The overall responder rate in the study eye.	Responder rate were defined as participants with a reduction in clinical activity score (CAS, see Secondary Outcome Measure 2 description for details) of = 2 points, and a reduction in proptosis of = 2 mm in the study eye, and no deterioration (increase in CAS of = 2 points or increase in proptosis of = 2 mm) in the non-study eye.)	Week12 and Week24 for phase II, Week 24 for phase III
Secondary	Percentage of subjects with a CAS value of 0 or 1 in the study eye.	According to the 7-item European Group on Graves' Ophthalmopathy (EUGOGO) amendment, CAS was used to evaluate clinical activity. For each of the following items, one point is given: spontaneous orbital pain, gaze evoked orbital pain, eyelid swelling that is considered to be due to active (inflammatory phase) Graves' ophthalmopathy (GO), eyelid erythema, conjunctival redness that is considered to be due to active (inflammatory phase) GO, chemosis, and inflammation of caruncle or plica. The sum of these points is the total score, with 0 indicating no clinical activity and 7 indicating the most severe clinical activity.	Week12 and Week24 for phase II, Week 24 for phase III
Secondary	Mean Change of the CAS value in the study eye.		Baseline to Week 12 and Week 24 for phase II
Secondary	Mean change from Baseline in proptosis measurement in the study eye.	proptosis measurement: see Primary Outcome Measure 1 description for details	Baseline to Week 12 and Week 24 for phase II, Baseline to Week 24 for phase III
Secondary	The proptosis responder rate of the study eye.	proptosis responder rate: see Primary Outcome Measure 1 description for details	Week 24 for phase II
Secondary	The diplopia responder rate of the study eye.		Week12 and Week24 for phase II, Week 24 for phase III