Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07062978

A Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia®

This study is a multicenter, randomized, double-blind comparative study to valuating the efficacy and safety of QL1206 and Prolia® in postmenopausal women with osteoporosis at high risk of fracture.

Recruiting

Interested in participating?

Request Info

Key information

Age range

50 year–85 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Zhejiang Provincial People's Hospital Bijie Hospital

Guizhou, China

Location status: Recruiting

Location contact

Jun Zhang

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects who agree to participate in the study and sign the informed consent form.
  • Postmenopausal women who can walk freely, aged 50-85 years (including 50 and 85 years old).
  • Subjects whose absolute value of bone mineral density (BMD) in the lumbar or total hip area meets T values ≤ -2.5 and > -4.0.
  • Subjects who must have at least one of the following risk factors: History of previous fragility fractures (occurring after the age of 40); history of hip fractures in fathers or mothers; increased bone turnover rate during screening; low body weight (BMI ≤ 19 kg/m2); advanced age (aged ≥ 65 years); current smoke.
  • The duration of spontaneous amenorrhea was >2 years or >2 years after bilateral oophorectomy. If the status of bilateral oophorectomy is unknown or if the ovaries are preserved after hysterectomy, follicle stimulating hormone (FSH) levels >40mIU/mL may be used to confirm the status of postoperative menopause.

Exclusion criteria

  • Bone/metabolic disease.
  • Hyperparathyroidism or hypoparathyroidism.
  • Thyroid condition: Hyperthyroidism or hypothyroidism.
  • Rheumatoid arthritis.
  • Malabsorption syndrome.
  • Renal disease - severe impairment of kidney function.
  • Vitamin D defViciency (25-hydroxyvitamin D, 25OHD <20 ng/mL).
  • Oral or dental diseases: previous or current evidence of mandibular osteomyelitis or osteonecrosis; Acute dental or mandibular disease requiring oral surgery; Planning invasive dental surgery; Failure to recover from dental or oral surgery.
  • Previously used denosumab drugs.
  • Use of intravenous bisphosphonates, fluoride, or strontium to treat osteoporosis within the last 5 years.
  • OOral bisphosphonates (used for at least 3 years, or used for less than 3 years but more than 3 months, with the last use occurring <1 year before the ICF).
  • Use of any of the following drugs within 6 weeks prior to screening that may affect bone metabolism.
  • History of more than two vertebral fractures.
  • Malignant tumors.

Treatment and study plan

QL1206

Drug

QL1206 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.

Prolia®

Drug

Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.

Primary outcomes

  1. Percent Change From Baseline in lumbar spine(LS)-BMD at Month 12

    Time frame: Baseline and 12 months

    Percent Change From Baseline in lumbar spine(LS)-BMD at Month 12

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Qilu Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Randomized, Double-blind Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia® in Postmenopausal Women With Osteoporosis at High Risk of Fracture

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jul 14, 2025
Registry last updated
Jul 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.