A Study to Evaluate LY06006 and Prolia in Healthy Adults

Luye Pharma Group

Status and phase: Unknown; Phase 1

Conditions: Healthy Adults

Treatments: Drug: LY06006; Drug: Prolia

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT04973722

LY06006/CT-CHN-103

Details and patient eligibility

About

A randomized, double-blind, parallel-group study in Chinese healthy male subjects to evaluate the pharmacokinetics, pharmacodynamics, safety and immunogenicity of LY06006 versus Prolia following single-dose subcutaneous injection

Full description

Study Design:

The study is a randomized, double-blind, parallel-group study in healthy adult male subjects to evaluate the pharmacokinetics, pharmacodynamics, safety and immunogenicity of LY06006 versus Prolia following single-dose subcutaneous injection.

A total of 168 healthy male subjects will be randomized 1:1 to receive a single subcutaneous (s.c.) injection of 60mg of either LY06006 ( LY06006 , 60 mg/1mL , Shandong Luye Pharmaceutical Co., Ltd.) or Prolia (60 mg / 1 mL , Amgen Inc.). During the entire study period, blood samples should be collected according to the Schedule of Assessments for pharmacokinetic, pharmacodynamic and immunogenicity analysis, and safety assessments should be conducted.

Enrollment: 168 patients

Sex: Male

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Voluntarily signed the informed consent form;
2. Healthy males，ages ≥18 to ≤50 years;
3. Body weight ≥58 to ≤68 kg and Body mass index (BMI) >18 to <28 kg/m2, body mass index (BMI) = weight ( kg ) / height 2 (m 2);
4. Normal or clinically acceptable vital signs, physical exams, laboratory tests, 12- lead ECG, abdominal color Doppler ultrasound, chest radiograph, etc. screening;
5. No pregnancy plans and voluntarily take effective contraceptive measures from the screening date to the end of the study .

Exclusion criteria

1. Prior diagnosis of bone disease, or any condition that will affect bone metabolism such as, but not limit to: malignant tumors ( including myeloma ), hypoparathyroidism / hyperthyroidism, hypothyroidism / hyperthyroidism, acromegaly, Cushing ' s syndrome, hypopituitarism, severe chronic obstructive pulmonary disease, rheumatoid arthritis, osteomalacia;
2. Prior history or current evidence of osteomyelitis or osteonecrosis of the jaw (ONJ), or risk factors for ONJ such as invasive dental surgery or jaw surgery during the trial, or unhealed dental or oral surgery wounds;
3. Recent bone fracture within 6 months;
4. Active and unhealed infections of the respiratory system, digestive system, urinary system, reproductive system, or skin;
5. Serum calcium of < Lower Limit of Normal (LLN) or > Upper Limit of Normal (ULN);
6. Prior use of medications affecting bone turnover before screening and for the duration of study, including but not limited to: denosumab, bisphosphonates or fluoride within 12 months, contraceptives containing estrogen, tibolone, estrogen, selective estrogen receptor modulators, aromatase inhibitors, calcitonin, strontium salts, parathyroid hormone (or derivatives), vitamin D supplements ( >1000 IU/ day), anabolic steroids, systemic glucocorticoids, calcitriol or similar, diuretics, anticonvulsants within 6 months; inhaled or topical glucocorticoid drugs within 2 weeks;
7. Allergy to more than two drugs or food, or allergy to the ingredients of the investigational medicinal product (IMP);
8. Blood donation or massive blood loss ( ≥200 mL ) within 3 months before screening ;
9. Any vaccination within 6 months before screening or for the duration of study;
10. Prior use of any prescription drugs, over-the-counter drugs, any vitamin products or herbal medicines within 14 days before screening ;
11. Intense physical exercise within 2 weeks before screening or for the duration of the study, or any other conditions affecting drug absorption, distribution, metabolism, and excretion;
12. Upon enquiry, prior smoke more than 5 cigarettes per day within 3 months before the study;
13. Upon enquiry, a history of alcohol abuse ( drinking more than 14 units of alcohol per week within the first three months prior to screening : 1 unit = 350 mL of beer, 45 mL of liquor, or 150 mL of wine ), or positive alcohol test;
14. Positive urine screen for drug or a history of drug abuse or drug use in the past five years upon questioning ;
15. Other diseases with clinical significance (such as nervous system, mental system , cardiovascular system, urinary system, digestive system, respiratory system, metabolic endocrine system, blood system, skin disease, immune disease, tumor, etc.);
16. Any of the following tests positive: hepatitis B surface antigen ( HBsAg ), hepatitis C antibody ( HCV-AB ), human immunodeficiency virus antigen antibody ( HIVAg / Ab ) and treponema pallidum antibody;
17. Acute diseases or concomitant medications from screening to IMP administration;
18. Consumption of any alcohol-containing products within 48 hours before administration of the IMP ;
19. Prior participation in clinical trials for denosumab or denosumab biosimilar products; current participation in other clinical studies, or receiving or have received any investigational drug within 3 months (or less than 5-half lives of that medication, whichever time period is longer) before receiving study drug ;
20. History of fainting blood or needles;
21. In the opinion of the investigator, others to be excluded.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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168 participants in 2 patient groups

LY06006

Experimental group

Description:

60 mg/1 ml, once every 6 months administered subcutaneously

Treatment:

Drug: LY06006

Prolia

Active Comparator group

Description:

60 mg/1 ml, once every 6 months administered subcutaneously

Treatment:

Drug: Prolia