A Long-Term Study with GLM101 in Patients with PMM2-CDG

Phase 1

• Conditions: PMM2-CDG; MedDRA version: 20.0Level: LLTClassification code: 10027426Term: Metabolic disorder NOS Class: 10027433; Therapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18]

• Registration Number: CTIS2024-512171-12-00
• Lead Sponsor: Glycomine Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-03-27
• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

Is willing and able to provide informed consent/assent, directly or through a legally authorized representative., Has successfully completed the Treatment Period with GLM101 in a previous clinical study., Ages 12-65 years, inclusive, at the time of signing the informed consent form (ICF)., If the participant is a female of childbearing potential (i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile (permanent sterilization methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy)) or becomes of childbearing potential during the study, she must not be pregnant (confirmed by a negative serum pregnancy test), is using a medically accepted method of contraception (abstinence, a hormonal contraceptive associated with inhibition of ovulation in conjunction with a barrier method or use of an intrauterine device), and must agree to continue using this method for 50 days after the last infusion of GLM101. Note: True abstinence: defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the subject. Periodic abstinence (such as calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception., If the participant is a female of non-childbearing potential, she must be pre-pubertal, surgically sterile, or must have an ovarian dysfunction confirmed by a follicle stimulating hormone (FSH) >40 IU/L. and absence of menses for 12 months without an alternative medical cause., If the participant is a sexually active (or becomes sexually active during the study) male with female partners, the sexually mature, nonsterile male participant agrees to use a medically acceptable method of contraception (abstinence, the partner taking a hormonal contraceptive in conjunction with a male condom or use by the partner of an intrauterine device with a male condom) and agrees to continue using this method for 50 days after the last infusion of GLM101. Males are considered surgically sterile if they have undergone bilateral orchiectomy or vasectomy at least 3 months prior to Screening., If the participant is male, he must agree to refrain from donating sperm during the study and 50 days after the last infusion of GLM101., Is willing and able to comply with this protocol.

Exclusion Criteria

Has any other condition that would, in the opinion of the Investigator, potentially compromise the safety or compliance of the participant or preclude the participant’s successful completion of the study., If female, has a positive serum pregnancy test during Screening., If female, must not be breastfeeding., Must not have a hypersensitivity to GLM101 or anti-histamine pre-medication, Participant is unwilling or unable to comply with scheduled visits, study drug administration plan, laboratory tests, other study procedures, and study restrictions.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified