Comparative Study to Evaluate the Efficacy and Safety of MYL-1701P and Eylea® in Subjects With Diabetic Macular Edema (DME)
Status and phase
Conditions
Treatments
Details and patient eligibility
About
Three hundred and twenty-four (324) eligible adult subjects with diabetes mellitus with central DME involvement to be randomized 1:1 to intravitreal treatment with MYL-1701P or Eylea®.
The primary endpoint is mean change from baseline in Best Corrected Visual Acuity (BCVA) as assessed by Early Treatment Diabetic Retinopathy Study (ETDRS) letters. Pharmacokinetics (PK) and immunogenicity to be evaluated in the subjects participating in the study.
Full description
Three hundred and twenty-four (324) eligible adult subjects with diabetes mellitus with central DME involvement to be randomized 1:1 to intravitreal treatment with MYL-1701P or Eylea®. Subjects to receive the assigned treatment until Week 48.
All subjects to return to clinic every 4 weeks to assess safety, efficacy and to guide treatment. Additional visits allowed during the study as specified in the study schedule for safety and pharmacokinetic evaluation.
Pharmacokinetics (PK) and Immunogenicity to be assessed in the subjects participating in the study.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
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Male or female subjects age ≥ 18 years.
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Subjects have type 1 or type 2 diabetes mellitus who present with central DME involvement in the study eye.
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The cause of decreased vision in the study eye has been attributed primarily to DME by the Investigator.
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Subject is able to understand and voluntarily provide written informed consent to participate in the study.
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If female of child bearing potential, the subject must have a negative serum pregnancy test at the Screening visit and a negative urine pregnancy test at baseline visit, and should not be nursing or planning a pregnancy.
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If female, subject must be:
- Surgically sterilized via hysterectomy, bilateral oophorectomy, or bilateral tubal ligation; or
- Of childbearing potential and practicing an acceptable form of birth control (defined as the use of an intrauterine device; a barrier method, like condom, with spermicide; any form of hormonal contraceptives; or abstinence from sexual intercourse) starting 60 days prior to dosing and continuing at least 90 days following the last treatment.
- Of non-childbearing potential (i.e., postmenopausal for at least 1 year).
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If male, subject must be surgically or biologically sterile. If not sterile, the subject must agree to use an acceptable form of birth control with sexual partner (as described in inclusion criteria #6b of protocol) or abstain from sexual relations during the study period and up to 90 days following the last treatment dose.
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Subject is willing to comply with the study duration, study visits and study related procedures.
Exclusion criteria
- Subjects with known hypersensitivity to aflibercept or any of the excipients
- Subjects with current or planned use of systemic medications known to be toxic to the lens, retina or optic nerve, including deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, phenothiazines and ethambutol
- Subjects with uncontrolled hypertension defined as systolic blood pressure >160mm Hg or diastolic blood pressure > 95 mm of Hg.
- Subjects with a history of cerebrovascular accident or myocardial infarction within 6 months of randomization.
- Subjects with history of use of intraocular corticosteroids anytime in the past or periocular (subconjunctival, intra-scleral, sub-tenon or retrobulbar) corticosteroids within 4 months of randomization
- Subjects who have only one functional eye, even if the eye met all other study requirements, or who have an ocular condition on the fellow eye with a poorer prognosis than the study eye.
Trial design
Primary purpose
Allocation
Interventional model
Masking
355 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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