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Treatment of Active Thyroid Eye Disease With MHB018A in a Randomized, Placebo-Controlled Study

2. juni 2026 opdateret af: Minghui Pharmaceutical (Hangzhou) Ltd

A Phase III, Randomized, Double-Masked, Placebo-Controlled Study to Evaluate the Efficacy of MHB018A Injection Treatment in Subjects With Active Moderate to Severe Thyroid Eye Disease.

The primary objective of this study is to evaluate the efficacy of MHB018A injection compared with placebo in participants with active moderate-to-severe TED.

Studieoversigt

Status

Ikke rekrutterer endnu

Detaljeret beskrivelse

The investigational drug, MHB018A, is a monoclonal antibody that inhibits the activity of a cell surface receptor called insulin-like growth factor-1 receptor (IGF-1R). Inhibition of IGF-1R may help to reduce the inflammation and associated tissue swelling that occurs in patients with thyroid eye disease (TED). The primary objective of this study is to evaluate the efficacy of MHB018A injection compared with placebo in participants with active moderate-to-severe TED.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

84

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  1. Subjects voluntarily participating in the study and signing the informed consent form;
  2. Aged 18-75 years (inclusive), of any gender;
  3. Clinical diagnosis of active Thyriod Eye Disease (TED). The Clinical Activity Score (CAS) of the study eye/target eye at screening and baseline must be ≥3 points (7-point scale).
  4. Subjects with a clinical diagnosis of moderate to severe TED at screening and baseline.
  5. Does not require immediate surgical ophthalmological intervention, and no corrective surgery/orbital radiotherapy is planned during the study.
  6. Diabetic subjects must have well-controlled stable disease.
  7. Sufficient bone marrow and organ function.
  8. Eligible subjects of childbearing potential (male and female) must agree to use reliable contraceptive methods; female subjects of childbearing potential must have a negative blood pregnancy test within 7 days before the first use of the study drug and must not be breastfeeding.
  9. Subject is willing and able to comply with the prescribed treatment protocol and evaluations for the duration of the study.

Exclusion Criteria:

  1. Decreased best corrected visual acuity due to optic neuropathy as defined by a decrease in vision within the last 6 months of two lines of Snellen chart, new visual field defect or color defect secondary to optic nerve involvement.
  2. Corneal decompensation unresponsive to medical management.
  3. Decrease in CAS of ≥ 2 points or decrease in proptosis of ≥ 2 mm between screening and baseline.
  4. Free thyroxine (FT4) and free triiodothyronine (FT3) levels <50% above or below the normal reference range at screening.
  5. Subjects who have previously received orbital radiotherapy or ophthalmic surgery for TED.
  6. Subjects who received oral or intravenous corticosteroids or corticosteroid eye drops/ointments for TED within 4 weeks before the first dose; subjects who received periorbital/orbital steroid injections within 3 months before the first dose.
  7. Subjects who used oral or intravenous corticosteroids for reasons other than TED within 4 weeks prior to Screening, excluding local use (topical, nasal, inhalation).
  8. Any previous treatment with rituximab, tocilizumab, other immunosuppressive agent use within 3 months prior to Screening.
  9. Previous treatment targeting IGF-1R.
  10. Selenium and biotin must be discontinued 3 weeks prior to Screening and must not be restarted during the trial; however, taking a multivitamin that includes selenium and/or biotin is allowed.
  11. Use of an investigational agent for any condition within 30 days prior to Screening or anticipated use during the course of the trial.
  12. Identified pre-existing ophthalmic disease that, in the judgment of the Investigator, would preclude study participation or complicate interpretation of study results.
  13. Malignant condition in the past 5 years before signing the ICF (except successfully treated basal/squamous cell carcinoma of the skin).
  14. Acute cardiovascular disease history or treatment within 6 months before the first dose.
  15. Presence of poorly controlled hypertension with systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg; Renal artery stenosis.
  16. Pregnant or lactating women.
  17. Drug or alcohol abuse during the screening period.
  18. Hearing impairment history in either ear during the screening period; or abnormal pure tone audiometry results.
  19. Biopsy-proven or clinically suspected inflammatory bowel disease.
  20. Positive results for serum virology tests (defined as pos
  21. Subjects who received or planned to receive live or attenuated live vaccines within 4 weeks before the first dose or during the study period.
  22. Subjects who underwent major surgery within 4 weeks before the first dose or are expected to undergo surgery during the study period or within 4 weeks after the study.
  23. Known hypersensitivity to any of the components of MNB018A or prior hypersensitivity reactions to mAbs.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: MHB018A
Patients with TED will be randomized to receive 6 subcutaneous injections of either MHB018A (450mg) or MHB018A placebo, once every 4 weeks (q4w)
MHB018A 450 mg til subkutan injektion en gang hver 4. uge (Q4W)
Placebo komparator: MHB018A Placebo
Patients with TED will be randomized to receive 6 subcutaneous injections of either MHB018A (450mg) or MHB018A placebo, once every 4 weeks (q4w)
6 subkutane injektioner af MHB018A placebo en gang hver 4. uge (Q4W)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Proptosis response rate at Week 24
Tidsramme: Week 24
The percentage of subjects with a reduction in proptosis of ≥2 mm in the study eye/target eye compared to baseline, without deterioration (≥2 mm) in the fellow eye.
Week 24

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Samlet svarprocent
Tidsramme: Uge 24
Procentdelen af ​​forsøgspersoner med ≥2-punkter i klinisk aktivitets score (CAS) reduktion og ≥2 mM reduktion i proptose fra baseline, forudsat at der ikke er nogen tilsvarende forringelse (≥2-point/mm stigning) i CAS eller proptosis i medens øje.
Uge 24
Ændring i propertose
Tidsramme: Baseline, op til uge 24
Ændring fra baseline i proptose i undersøgelsesøjet målt ved exophthalmometer i uge 24
Baseline, op til uge 24
Diplopia -svarprocent
Tidsramme: Uge 24
Procentdelen af ​​forsøgspersoner med en reduktion i diplopi -sværhedsgraden med ≥1 klasse.
Uge 24
Farmakokinetisk parametertrugkoncentration for MHB018A
Tidsramme: Op til uge 24
Trough-koncentration (CTROUGH) vil blive vurderet ved anvendelse af ikke-komparten metoder hos deltagere, der er randomiseret til MHB018A-gruppen.
Op til uge 24
Anti-MHB018A antistof (ADA) forekomst
Tidsramme: Op til uge 24 og ved slut-af-prøve (EOT) besøg
Procentdelen af ​​forsøgspersoner, der udvikler anti-MHB018A-antistoffer.
Op til uge 24 og ved slut-af-prøve (EOT) besøg
Percentage of subjects with CAS of 0 or 1
Tidsramme: Week 24
The percentage of subjects with a CAS (Clinical Activity Score) of 0 or 1 in the study eye/target eye. CAS ranges from 0 to 7, while higher scores mean a worse outcome.
Week 24
Change in CAS
Tidsramme: Week 24
The mean change from baseline to Week 24 in the CAS (Clinical Activity Score) in the study eye/target eye. CAS ranges from 0 to 7, while higher scores mean worse outcome.
Week 24
Change in Quality of Life (GO-QOL) Scores
Tidsramme: Week 24
The mean change in scores from the Graves' Ophthalmopathy Quality of Life questionnaire compared to baseline. The GO-QoL is a self-filled questionnaire containing 16 items. The raw scores for items 1-8 and items 9-16 are summed separately, each yielding a total raw score ranging from 8 to 24. Each raw score is then transformed into a 0-100 scale using the following formula: Total Score = (Raw Score - 8) ÷ 16 × 100. Higher scores indicate better quality of life.
Week 24

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. december 2026

Primær færdiggørelse (Anslået)

1. juli 2028

Studieafslutning (Anslået)

1. juli 2029

Datoer for studieregistrering

Først indsendt

27. maj 2026

Først indsendt, der opfyldte QC-kriterier

27. maj 2026

Først opslået (Faktiske)

2. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

4. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. juni 2026

Sidst verificeret

1. juni 2026

Mere information

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Kliniske forsøg med MHB018A

Abonner