Safety and Tolerability of Intravenous LLP2A-Alendronate for Osteopenia Secondary to Glucocorticoids

Completed · Phase 1 · Has a placebo group

Conditions studied: Osteopenia, Osteoporosis, Osteonecrosis

In brief

A Phase 1 Randomized, Double-Blind, Placebo-Controlled Single and Multiple Ascending Dose Study of the Safety and Tolerability of Intravenous LLP2A-Alendronate in Adult Men and Women with Osteopenia Secondary to Corticosteroids

Key facts

Study ID

NCT03197623

Run by

Nancy E. Lane, MD

People needed

58

Starts

2016-10-14

Expected to finish

2021-03-31

Last updated by the study team

2021-08-06

Who can join

Age: 20 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must meet all of the following criteria to be included in the study.
• 20 - 85 years old
• Receiving 5 - 40 mg/day prednisone, or equivalent of another GC (methylprednisolone 4 mg/day, or prednisone 10 mg every other day) for a minimum of 4 consecutive weeks prior to enrollment
• Anticipated to continue to receive at least 5 mg/day prednisone or equivalent throughout study participation
• T score ≤ -1.0 in the femoral neck or total hip or lumbosacral spine. Only one result from one of these locations that is ≤ -1.0 is required. For screening DXA, a DXA completed within 6 months of screening may be used; otherwise DXA must be completed within 4 weeks of screening visit.
• Must be ambulatory and able to attend all appointments
• Women must agree to use one of the following methods of birth control for the duration of the clinical trial: systemic hormonal contraceptive (oral, injected, transdermal), intrauterine device, double barrier (e.g., cervical cap or diaphragm with condom or spermicide). Men with female partners must agree to use double barrier contraception, unless their partner is using systemic hormonal contraceptives or has an intrauterine device.
• In the opinion of the investigator, the concurrent medical conditions of the study subject are stable
• Subject undergoing PET/CT scans must have the ability to lay motionless for up to 30-45 minutes
• Anticipated to continue to receive all chronic medications without dose changes throughout study participation
• Subjects undergoing PET/CT scans must have the ability to lay motionless for up to 30-45 minutes

You may not qualify if…

• Subjects who meet any of the following criteria will be excluded from the study:
• Weight greater than the limit of the DXA table at the clinical site
• History or concurrent conditions that might place the subject at increased risk, such as renal insufficiency (CKD 4 or 5), glomerulonephritis, atypical infections due to impaired immunity, hypersensitivity to multiple IV medications
• History of or concurrent presence of medical conditions which might interfere with ability to participate for the duration of the study, such as clinically significant cardiovascular disease, uncontrollable hypertension, uncontrolled asthma, symptomatic pulmonary fibrosis, recent GI bleeding requiring transfusion, psychosis, substance abuse or hospital admission within 6 months of enrollment (except for elective procedures)
• Prior use or current need for prohibited concomitant medications
• Rheumatic disease with clinically significant renal or central nervous system involvement
• History of deep vein thrombosis (DVT) along with taking any prophylaxis/treatment that occurred within the last 5 years
• History of clinically significant atrial fibrillation and/or taking medications for its treatment and prevention
• Unable or unwilling to comply with restrictions on alcohol 9. Previous hypersensitivity to alendronate
• Any of the following on Screening laboratory tests:
• Total calcium values outside the normal range (corrected if albumin < lower limit of normal (LLN))
• Phosphate level < LLN
• 25-hydroxyvitamin D (25-OH Vitamin D) below 10ng/mL
• TSH > upper limit of normal (ULN)
• Hepatic enzymes (ALT, AST, GGT) > 1.5 X ULN
• Creatinine clearance (eGRF) <35 mL/min/1.73 m2 using the Modification of Diet in Renal Disease (MDRD) formula
• Hemoglobin <10 g/dL
• Positive serology for HIV, Hepatitis B or C
• Positive pregnancy test
• Prolonged QTc interval (QTcF (Fredericia) of > 450 msec for men, > 470 msec for women)
• Any other clinically significant laboratory value as judged by the investigator 11. Subject cannot enroll in MAD part of study until after 60 days of completing SAD part of study 12. Subjects undergoing PET/CT scans must not be breast-feeding 13. History of hypersensitivity to fluoride

Where it is running

• West Coast Clinical Trials (WCCT) — Cypress, California, United States
• Diablo Clinical Research — Walnut Creek, California, United States
• Altoona Center for Clinical Research — Duncansville, Pennsylvania, United States
• Metroplex Clinical Research Center — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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