G56W1 in Women With Postmenopausal Osteoporosis

Two-dose, Positive Drug Control, Multicentre, Randomized, Double-blind Study of Recombinant Human Parathyroid Hormone for Injection(rhPTH)(1-34) Once a Week to Treat Postmenopausal Osteoporosis Women for the Evaluation the Pharmacokinetics and Safety and to Explore Therapeutic Effects

This study will assess the pharmacokinetics and safety and explore therapeutic effects with once-weekly recombinant human parathyroid hormone for injection ( 1-34 ) ( G56W1 ) in women with post-menopausal osteoporosis .The anticipated time on study treatment is 24 weeks, and the target sample size is 148 individuals.

Study Overview

• Status: Unknown
• Conditions: Postmenopausal Osteoporosis
• Intervention / Treatment: Biological: rhPTH（1-34） 28.2μg; Biological: rhPTH（1-34） 56.5μg; Biological: teriparatide acetate(Teribone™)

• Study Type: Interventional
• Enrollment (Anticipated): 148
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• China
  • Beijing
    • Beijing, Beijing, China, 100006
      • Peking Union Medical College Hospital
  • Chongqing
    • Wanzhou, Chongqing, China
      • Chongqing Three Gorges Central Hospital
  • Jiangsu
    • Nanjing, Jiangsu, China
      • Nanjing Drum Tower Hospital
    • Nanjing, Jiangsu, China
      • Zhongda Hospital, Southeast University
  • Shanghai
    • Shanghai, Shanghai, China
      • Shanghai sixth people's hospital
    • Shanghai, Shanghai, China, 200000
      • Huadong Hospital affiliated to Fudan University
  • Sichuan
    • Chengdu, Sichuan, China
      • West China Hospital,Sichuan University
    • Chengdu, Sichuan, China
      • The West China Second UniversityHospital of Sichuan University
  • Tianjin
    • Tianjin, Tianjin, China
      • Tianjin Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 45 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Female, capable of self - motivation , 45 years old ≤ age ≤ 75 years old.
• Natural menopause for 3 years or more; or surgical menopause for 3 years or more (surgery needs to be performed after 40 years old), for women with surgical menopause, estradiol(E2)< 25 pg/ml and follicle stimulating hormone(FSH) > 40mIU/ml should be met.
• Weight ≥ 40kg , 18 ≤ body mass index(BMI)≤ 30 .

• Meets one of the following diagnostic criteria for osteoporosis, and ≥ 3 vertebral bodies of L1-4 can be measured by bone mineral density using the DXA method.

  1. Brittle fracture of the hip or vertebral body, and the bone density measurement T- score< -1.0.
  2. The T- score of the central axis bone mineral density or the 1/3 bone density of the distal radius of the tibia was ≤-2.5 measured by DXA .
  3. Bone density measurements were consistent with low bone mass ( -2.5 < T- value < -1.0 ) and combined with proximal humerus, pelvic or forearm distal brittle fractures.
• to participate in the trial and sign the informed consent form.

Exclusion Criteria:

• to have diseases affecting calcium or bone metabolism that are not effectively controlled, such as primary hyperparathyroidism or hyperthyroidism, Paget's bone disease, hypercalcemia, hypocalcemia, active urolithiasis.
• Secondary osteoporosis, such as osteomalacia, rheumatoid arthritis, gout, multiple myeloma, etc.
• Severe lumbar anatomical abnormalities which affecting DXA bone mineral density measurement, such as severe scoliosis.

• Patients who have been treated for anti-osteoporosis before random enrollment:

  1. Patients who received parathyroid hormone(PTH) therapy before random enrollment (including clinical trials of similar products).
  2. Patients who received bisphosphonate injection within 1 year prior to random enrollment or received bisphosphonate oral administration within 3 months for > 2 weeks prior to enrollment.
  3. Systemic treatment of androgen, estrogen, and selective estrogen receptor modulator(SERM) preparations within 3 months > 2 weeks prior to random enrollment.
  4. Three months before randomized to receive of heparin, warfarin, anticonvulsants (except benzodiazepines), digoxin accumulated for> 2 weeks.
  5. In the 3 months prior to random enrollment , received calcitonin, vitamin K preparation, active vitamin D3 preparation, oral or intravenous glucocorticoid treatment for > 4 weeks.
• Suffering from severe kidney disease, uncontrolled high blood pressure ( ≥150/100 mmHg ), symptomatic ischemic heart disease, cerebral infarction or obliterative atherosclerosis, malignancy, and other serious underlying diseases.

• Laboratory tests indicates abnormal, including any of the following indicators abnormalities (according to the normal range of each center, after consideration of the investigator with clinical considerations, such as caused by operational procedures, etc., after discussion with the sponsor, may allow retesting once) .

  1. Alkaline phosphatase(ALP)>1.5 times the upper limit of normal.
  2. Aspartate transaminase(AST) or alanine aminotransferase(ALT) or total bilirubin(TBIL) > 2.0 times the upper limit of normal.
  3. Glycated hemoglobin(HbA1c )≥ 7.0% .
  4. White blood cell(WBC)< 3.5×10^9 /L , Hb<100g/L or Plt<90×10^9 /L.
  5. Thyroid-stimulating hormone(TSH)<0.01 mIU/L (mU/L) or TSH>10 mIU/L (mU/L) .
  6. Parathyroid hormone(PTH)>1.5 times the upper limit of normal.
  7. Serum creatinine(SCr)>1.2 times the upper limit of normal.
  8. Serum total calcium(SCa)> normal upper limit.
• Subjects who had significant clinical significance including HIV , hepatitis B, hepatitis C, and syphilis ( hepatitis B virus carriers can be enrolled ) .
• Heavy Smoking (average of more than 10 / day) and / or alcohol addicted (converted to pure alcohol 30 ml / day or more) .
• Recent drug abuse or drug dependence evidence.
• Those who are allergic to test drugs / control drugs or biological products.
• Included in other interventional clinical trials within 3 months of the study.
• Been undergone radiation therapy for bones.
• Mental illness or any cause of cognitive impairment.
• Patients who were considered unsuitable for the study based on risk benefits by investigators.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: rhPTH（1-34） 28.2μg; Participants received 28.2μg rhPTH（1-34）administered by subcutaneous injection once a week for 24 weeks.	Biological: rhPTH（1-34） 28.2μg; Administered by subcutaneous injection; Other Names: G56W1
Experimental: rhPTH（1-34） 56.5μg; Participants received 56.5μg rhPTH（1-34）administered by subcutaneous injection once a week for 24 weeks.	Biological: rhPTH（1-34） 56.5μg; Administered by subcutaneous injection; Other Names: G56W1
Active Comparator: teriparatide acetate(Teribone™); Participants received 56.5μg teriparatide acetate(Teribone™) administered by subcutaneous injection once a week for 24 weeks.	Biological: teriparatide acetate(Teribone™); Administered by subcutaneous injection

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The percentage change in bone density of the lumbar spine ( L1-4 ) from baseline to 24 weeks after treatment	bone mineral density(BMD) measured by dual energy x-ray absorptiometry (DXA)	Baseline，week 24

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Evaluate the rate of change of Procollagen I N-terminal peptide(PINP),Serum cross-linked C-terminal telopeptide of type I collagen(s-CTX) ,Bone alkaline phosphatase(BALP) , and blood calcium from baseline	Central lab will be used	Baseline，week 24
The percentage change of total hip bone density from baseline to 24 weeks after G56W1 treatment	BMD measured by DXA	Baseline，week 24
Maximum plasma concentration (Cmax)	serum parathyroid hormone(PTH) will be tested for all pharmacokinetics parameters	Baseline，week 1，week 4，week 12，week 24
Area under the plasma concentration versus time curve (AUC)	serum PTH will be tested for all pharmacokinetics parameters	Baseline，week 1，week 4，week 12，week 24
Time to maximum plasma concentration（Tmax）	serum PTH will be tested for all pharmacokinetics parameters	Baseline，week 1，week 4，week 12，week 24
Elimination half-life（t1/2）	serum PTH will be tested for all pharmacokinetics parameters	Baseline，week 1，week 4，week 12，week 24

Collaborators and Investigators

• Sponsor: Shenzhen Salubris Pharmaceuticals Co., Ltd.
• Investigators: Principal Investigator: Weibo Xia, Prof., Peking Union Medical College

Study record dates

Study Major Dates

• Study Start (Actual): October 1, 2018
• Primary Completion (Anticipated): May 31, 2020
• Study Completion (Anticipated): August 31, 2020

Study Registration Dates

• First Submitted: October 14, 2018
• First Submitted That Met QC Criteria: October 23, 2018
• First Posted (Actual): October 25, 2018

Study Record Updates

• Last Update Posted (Actual): October 25, 2018
• Last Update Submitted That Met QC Criteria: October 23, 2018
• Last Verified: October 1, 2018

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Metabolic Diseases; Musculoskeletal Diseases; Bone Diseases; Bone Diseases, Metabolic; Osteoporosis; Osteoporosis, Postmenopausal; Physiological Effects of Drugs; Bone Density Conservation Agents; Calcium-Regulating Hormones and Agents; Teriparatide
• Other Study ID Numbers: G56W1A201

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No