A Study of IBI311 in Subjects With Steroid-resistant, Thyroid Associated Ophthalmopathy

NCT06269393 | Completed Phase 3

• 1 other identifier: CIBI311Y101
• Study Type: interventional
• Target: 53
• Locations: 1 country
• Sites: 1

Brief Summary

This is an exploratory study of the efficacy and safety of IBI311, a modified anti-IGF-1R antibody, in patients with steroid-resistant, thyroid associated ophthalmopathy (TAO). This study includes two stages. Stage I is a single-center, single-arm, open-label clinical study designed to evaluate the safety and tolerability of IBI311 in subjects with TAO. Approximately 10 subjects meeting the study eligibility criteria will be enrolled. Stage II is a single-center, randomized, double-masked, placebo-controlled clinical trial designed to evaluate the efficacy and safety of IBI311 in subjects with steroid-resistant TAO. Approximately 54 subjects meeting the study eligibility criteria will be randomly assigned to IBI311 or placebo on day 1 (D1) in a 2:1 ratio stratified by disease activity.

Conditions

Thyroid Associated Ophthalmopathy

Outcome Measures

Primary Outcomes (1)

• The proptosis responder rate (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) of the study eye.

  Proptosis assessment: proptosis of the study eye as measured by Hertel exophthalmometer.

  Week 12

Secondary Outcomes (3)

• Overall responder rate in proptosis of the study eye.

  Weeks 12 and 24

• Percentage of subjects with a CAS value of 0 or 1

  Weeks 12 and 24

• Diplopia responder rate (defined as percentage of subjects with a ≥ 1-grade improvement in diplopia)

  Weeks 12 and 24

Other Outcomes (1)

• Safety and tolerability of intravenous IBI311 in subjects with TAO

  Up to 24 weeks

Study Arms (2)

Placebo

PLACEBO COMPARATOR

Participants with TAO will be randomized to receive 4 intravenous infusions of placebo with an interval of 3 weeks, followed by 4 intravenous infusions of IBI311 with an interval of 3 weeks.

Drug: Placebo

IBI311

ACTIVE COMPARATOR

Participants with TAO will be randomized to receive 8 intravenous infusions of IBI311 with an interval of 3 weeks.

Drug: IBI311

Interventions

Placebo DRUG

Placebo group: 10 mg/kg of placebo on Day 1, followed by 20 mg/kg, q3W of placebo for the following 3 infusions.10 mg/kg of IBI311 at Week 12, followed by 20 mg/kg, q3W of IBI311 for the remaining 3 infusions.

Placebo

IBI311 DRUG

IBI311 group: 10 mg/kg of IBI311 on Day 1, followed by 20 mg/kg, q3W of IBI311 for the remaining 7 infusions; .

IBI311

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent.
• Male or female subject between 18 and 80 years (inclusive) at Screening.
• Steroid-resistant TAO, defined as poor response to steroid after completing a 3-month steroid pulse therapy (4.5g to 8.0g methylprednisolone) or 3-6 months of oral glucocorticoids treatment (i.e., CAS decreased by \< 2 points, or proptosis decreased by \< 2mm, or no improvement in diplopia), or relapse of TAO after steroid withdrawal (CAS increased by ≥2 points and CAS≥3 points \[7-item scale\] in either eye, or proptosis increased by ≥2 mm, or Gorman diplopia score increased by ≥1 point).
• Moderate-to-severe active TAO or chronic TAO at screening:
• Active TAO, with CAS ≥3 in the study eye during the screening period;
• Proptosis ≥18 mm in the study eye;
• Moderate to severe active TAO, usually associated with at least two of the following manifestations: eyelid retraction ≥ 2 mm, moderate or severe soft tissue involvement, proptosis ≥ 3 mm above upper limit of normal (ULN), inconstant or constant diplopia (Gorman subjective diplopia score 2-3);
• CAS ≤2 in both eyes during the screening period;
• Proptosis ≥18 mm in the study eye;
• A clinical diagnosis of chronic non-active TAO at screening was defined as CAS ≤2 in both eyes for at least 6 months prior to screening, or having all of the following characteristics: no progression of proptosis, no newly onset diplopia or diplopia progression induced by TED at least 6 months prior to screening, and no new inflammatory TAO symptoms.
• Infertile female subjects or fertile female subjects with negative blood pregnancy test results during the screening period and agrees to take contraceptive measures from screening to 120 days after the last dose; male subjects should agree to use contraceptive measures from screening to 120 days after the last dose.

You may not qualify if:

• Subjects will be ineligible for study participation if they meet any of the following criteria:
• Decreased best-corrected visual acuity due to optic neuropathy (defined as a ≥ 2-line decrease in best-corrected visual acuity due to optic neuropathy within the past 180 days), newly emerging visual field defects or color vision impairment secondary to optic nerve damage;
• Subjects with corneal ulcer;
• Immediate orbital radiotherapy or orbital decompression as judged by investigators;
• Orbital radiation therapy or surgical treatment for TAO, including orbital decompression, strabismus diorthosis and eyelid diorthosis, at any time before baseline, or planned to have the aforementioned treatments during the study;
• Subjects with poorly controlled thyroid function, defined as FT3 or FT4 levels deviating from the normal reference ranges of the local study site laboratories by more than 50% at screening;
• Receiving Teprotumumab or IBI311 at any time before baseline;
• Receiving anti-CD20 antibody or interleukin-6 receptor antibody treatment within 180 days prior to baseline;
• Oral or intravenous administration of any other non-steroid immunosuppressant within 90 days prior to baseline

Sponsors & Collaborators

• Peking University People's Hospital: lead

Study Sites (1)

Peking University People's Hospital

Beijing, Beijing Municipality, 100034, China

Location

MeSH Terms

Conditions

Graves Ophthalmopathy

Condition Hierarchy (Ancestors)

Eye Diseases, Hereditary; Eye Diseases; Graves Disease; Exophthalmos; Orbital Diseases; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Goiter; Thyroid Diseases; Endocrine System Diseases; Hyperthyroidism; Autoimmune Diseases; Immune System Diseases

Study Officials

• Wenhui Ren

  Peking University People's Hospital Research Office

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: associate chief physician

Study Record Dates

• First Submitted: January 25, 2024
• First Posted: February 21, 2024
• Study Start: January 1, 2024
• Primary Completion: April 3, 2025
• Study Completion: July 3, 2025
• Last Updated: March 24, 2026

Record last verified: 2026-03

Locations

CN (1)