Safety, Pharmacokinetics and Efficacy of MBX 2109 in Patients With Hypoparathyroidism

NCT ID: NCT06465108

Last Updated: 2025-10-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 64 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-08-08
• Study Completion Date: 2025-06-04

Brief Summary

The purpose of this study is to investigate the safety and tolerability of MBX 2109 administered once weekly to patients with hypoparathyroidism.

Detailed Description

This study is to investigate the safety, pharmacokinetics, and efficacy of MBX 2109 administered once weekly to patients with hypoparathyroidism. Given MBX 2109 is intended as a PTH replacement hormone to demonstrate that MBX 2109 can maintain serum calcium within a normal range without the need for active vitamin D and therapeutic calcium supplements.

Conditions

Hypoparathyroidism

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Starting dose of 400 µg once-weekly by subcutaneous injection

Group Type: EXPERIMENTAL

MBX 2109

Intervention Type: DRUG

Supplied as 1.5 mg per vial reconstituted in 1.4 mL water for injection to a concentration of 1.0 mg/mL

Starting dose of 600 µg once-weekly by subcutaneous injection

Group Type: EXPERIMENTAL

MBX 2109

Intervention Type: DRUG

Supplied as 1.5 mg per vial reconstituted in 1.4 mL water for injection to a concentration of 1.0 mg/mL

Starting dose of 800 µg once-weekly by subcutaneous injection

Group Type: EXPERIMENTAL

MBX 2109

Intervention Type: DRUG

Supplied as 1.5 mg per vial reconstituted in 1.4 mL water for injection to a concentration of 1.0 mg/mL

Placebo - once-weekly by subcutaneous injection

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Supplied in 1.4 mL water for injection

Interventions

MBX 2109

Supplied as 1.5 mg per vial reconstituted in 1.4 mL water for injection to a concentration of 1.0 mg/mL

Intervention Type: DRUG

Placebo

Supplied in 1.4 mL water for injection

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Is an adult ≥18 years of age at the time of the Screening visit.

a. If ≤25 years of age, radiological evidence of epiphyseal closure based on X-ray of non-dominant wrist and hand

2. Has a diagnosis of one of the following types of hypoparathyroidism for at least 26 weeks prior to the Screening visit:

1. Postsurgical chronic hypoparathyroidism

2. Idiopathic hypoparathyroidism

3. Autoimmune hypoparathyroidism (e.g., isolated autoimmune hypoparathyroidism; stable, well-managed patients with autoimmune polyglandular syndrome type 1/autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy without current or past malabsorption at the discretion of the principal investigator [PI])

3. On a dose for at least 4 weeks prior to the Screening visit of the following:

1. Calcitriol ≥0.5 µg per day or alfacalcidol ≥1 ug per day (active vitamin D)

2. Elemental calcium (citrate or carbonate) supplement ≥800 mg per day

a) If the patient had a history of hypercalcemia on the above active vitamin D and/or calcium doses, the patient may be eligible to participate in the study on lower doses of calcitriol, alfacalcidol and/or elemental calcium with approval of the medical monitor

4. At the Screening visit or at completion of the Optimization Period, the following serum analytes must be within the following ranges:

• AdjCa: 8.2 to 10.6 mg/dL (2.05 to 2.65 mmol/L), inclusive, targeting the lower half of the reference range
• 25 (OH)D: 30 to 64 ng/mL (75 to 160 nmol/L), inclusive
• Magnesium: within the normal range of 1.8 to 2.6 mg/dL (0.65 to 1.05 mmol/L; 1.3 mEq/L to 2.1 mEq/L), inclusive; if the patient had a history of not being successful in maintaining serum magnesium within the normal reference range, a level slightly below the normal range (≥1.3 mg/dL [≥0.53 mmol/L]) may be acceptable with approval by the medical monitor 1.3 mEq/L to 2.1 mEq/L), inclusive

5. Has an estimated glomerular filtration rate >60 mL/min/1.73 m2, as estimated using the Chronic Kidney Disease Epidemiology Collaboration equation, at the Screening visit.

6. Has thyroid-stimulating hormone (TSH) within normal laboratory limits prior to randomization. If patient is on thyroid medication, the dose should be stable for at least 4 weeks. If TSH is not within normal limits at screening, the dose of thyroid medication may be adjusted and TSH repeated in 4 weeks. If receiving suppressive therapy for a history of (differentiated) thyroid cancer, TSH level must be ≥0.2 mIU/L.

7. Can comprehend and is willing to sign an informed consent form (ICF) and to abide by the study restrictions, study visits, and procedures.

Exclusion Criteria

1. Has a known history of pseudohypoparathyroidism (impaired responsiveness to PTH, which is characterized as PTH-resistance, with elevated PTH levels in the setting of hypocalcemia).

2. Has any disease (other than hypoparathyroidism) that might affect calcium metabolism or calcium-phosphate homeostasis or PTH levels (e.g., disorders of the calcium sensing receptor [e.g., autosomal dominant hypocalcemia type 1] are exclusionary).

3. Use any of the following therapies:

1. Loop diuretics, thiazide diuretics, phosphate binders (other than calcium carbonate or citrate), digoxin, lithium, methotrexate, raloxifene hydrocholoride, or acute systemic corticosteroids within 4 weeks prior to the Screening Visit;

• Chronic systemic corticosteroid use is allowed if the dose has been stable for 4 weeks prior to Screening visit

2. PTH or PTH-related protein drugs such as PTH(1-84) and PTH(1-34) within 4 weeks of the Screening visit;

3. Oral or intravenous bisphosphonates, denosumab, or romosozumab-aqqg within 18 months of the Screening visit; or

4. Other drugs known to influence calcium and bone metabolism such as calcitonin, fluoride tablets (>0.5 mg per day), strontium or cinacalcet hydrochloride within 3 months of the Screening visit.

4. Had a non-hypocalcemic seizure within 6 months of the Screening visit. Note: a history of seizures that occur in the setting of hypocalcemia is not exclusionary

5. Is at an increased risk for osteosarcoma (e.g., Paget's disease, prior history of substantial external beam or implant radiation therapy involving the skeleton, unexplained elevations of alkaline phosphatase)

6. Is affected by active or uncontrolled disease processes that may adversely affect gastrointestinal absorption at the discretion of the PI.

7. Has a history of an active or untreated malignancy or are in remission from a clinically significant malignancy (other than differentiated thyroid cancer, basal or squamous cell skin cancer, in situ carcinomas of the cervix, or in situ prostate cancer) for less than 2 years from the Screening visit.

8. Has any clinically significant cardiovascular disease within 6 months prior to the Screening visit such as symptomatic heart failure, an acute coronary syndrome, uncontrolled arrhythmia, or cerebrovascular accident.

9. Has a clinically significant abnormal 12-lead ECG in the opinion of the investigator at the Screening visit suggestive of underlying cardiac disease.

10. Has a seated systolic blood pressure <100 mmHg or >165 mmHg and/or diastolic blood pressure >100 mmHg at the Screening visit. If outside this range, measurement can be repeated on another day for eligibility purposes within the Screening Period. If on medications for hypertension, the doses should be stable for 4 weeks prior to the Screening visit.

11. Has a history of symptomatic nephrolithiasis within 3 months of the Screening visit.

12. Has an episode of acute gout within 2 months of the Screening visit.

13. Has any major surgery performed within the 6 months prior to the Screening visit or plans to have surgical procedures that might interfere with the patient's ability to complete the study.

14. Is pregnant, lactating or a woman of childbearing potential (WOCBP) who plans to conceive during the study.

1. WOCBP must use at least 2 highly effective methods of contraception throughout the study and for 6 weeks following administration of the last dose of study drug.

2. A heterosexually active male patient and his female partner(s) of childbearing potential must agree to use 2 effective birth control methods for the duration of the study and for 90 days after the last dose of study drug. A male patient must agree to refrain from sperm donation from the date of screening until 90 days after his last dose of study drug.

15. Has any disease or condition that, in the opinion of the investigator, may make the patient unlikely to fully complete the study, or any condition that presents undue risk from the investigational product or procedures.

16. Has a known allergy or sensitivity to PTH or any of the excipients used in MBX 2109.

17. Has a diagnosis of drug or alcohol dependence within 12 months prior to the Screening visit.

18. Has participated in any other interventional trial in which the patient received an investigational drug within 2 months or within 5 half-lives of the investigational drug (whichever is the longest) prior to the Screening visit.

19. Has any other reason that, in the opinion of the investigator, would prevent the patient from completing participation or following the study schedule.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MBX Biosciences

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

MBX Biosciences Investigational Site

Sacramento, California, United States

MBX Biosciences Investigational Site

Jacksonville, Florida, United States

MBX Biosciences Investigational Site

Jacksonville, Florida, United States

MBX Biosciences Investigational Site

Miami, Florida, United States

MBX Biosciences Investigational Site

Macon, Georgia, United States

MBX Biosciences Investigational Site

Chicago, Illinois, United States

MBX Biosciences Investigational Site

Chicago, Illinois, United States

MBX Biosciences Investigational Site

Jackson, Mississippi, United States

MBX Biosciences Investigational Site

St Louis, Missouri, United States

MBX Biosciences Investigational Site

Omaha, Nebraska, United States

MBX Biosciences Investigational Site

Las Vegas, Nevada, United States

MBX Biosciences Investigational Site

Reno, Nevada, United States

MBX Biosciences Investigational Site

Albany, New York, United States

MBX Biosciences Investigational Site

Great Neck, New York, United States

MBX Biosciences Investigational Site

New York, New York, United States

MBX Biosciences Investigational Site

The Bronx, New York, United States

MBX Biosciences Investigational Site

Greenville, North Carolina, United States

MBX Biosciences Investigational Site

Cleveland, Ohio, United States

MBX Biosciences Investigational Site

Columbus, Ohio, United States

MBX Biosciences Investigational Site

Philadelphia, Pennsylvania, United States

MBX Biosciences Investigational Site

Dallas, Texas, United States

MBX Biosciences Investigational Site

El Paso, Texas, United States

MBX Biosciences Investigational Site

Fort Worth, Texas, United States

MBX Biosciences Investigational Site

Round Rock, Texas, United States

MBX Biosciences Investigational Site

San Antonio, Texas, United States

MBX Biosciences Investigational Site

Weslaco, Texas, United States

MBX Biosciences Investigational Site

Madison, Wisconsin, United States

MBX Biosciences Investigational Site

CABA, Buenos Aires, Argentina

MBX Biosciences Investigational Site

CABA, Buenos Aires, Argentina

MBX Biosciences Investigational Site

Río Cuarto, Córdoba Province, Argentina

MBX Biosciences Investigational Site

Córdoba, , Argentina

MBX Biosciences Investigational Site

San Miguel de Tucumán, , Argentina

MBX Biosciences Investigational Site

Samsun, , Turkey (Türkiye)

Countries

United States; Argentina; Turkey (Türkiye)

Other Identifiers

MBX-2H1002

Identifier Type: -

Identifier Source: org_study_id