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A Study to Evaluate the Efficacy and Safety of LY06006 in Postmenopausal Women With Osteoporosis at High Risk for Fracture

17. september 2021 oppdatert av: Luye Pharma Group Ltd.

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of LY06006 in Postmenopausal Women With Osteoporosis at High Risk for Fracture

A multicenter, randomized, double-blind, placebo-controlled phase III clinical study will be conducted to evaluate the efficacy and safety of LY06006 in the treatment of postmenopausal women with osteoporosis at high risk for fracture, as well as an exploratory population pharmacokinetic analysis of LY06006.

Studieoversikt

Status

Rekruttering

Intervensjon / Behandling

Detaljert beskrivelse

It is a multicenter, randomized, double-blind, placebo-controlled phase III clinical trial.

Primary Objective:

To evaluate the efficacy of LY06006 in the treatment of postmenopausal women with osteoporosis at high risk for fracture.

Secondary Objectives:

To evaluate the safety of LY06006. To evaluate the immunogenicity of LY06006. Population pharmacokinetic analysis of LY06006.

Studietype

Intervensjonell

Registrering (Forventet)

448

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • Shanghai
      • Shanghai, Shanghai, Kina, 200233
        • Rekruttering
        • Shanghai Sixth People's Hospital
        • Ta kontakt med:
        • Hovedetterforsker:
          • Zhenlin Zhang, doctor
        • Underetterforsker:
          • Jiemei Gu, doctor

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

50 år til 85 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  1. Postmenopausal woman, ages ≥50 to ≤85 years.≥3 years postmenopausal, which can be≥3 years of spontaneous amenorrhea or ≥3 years post-surgical bilateral oophorectomy. If < 60 years of age and had hysterectomy but ovarian retention, require follicle stimulating hormone (FSH) levels ≥40U/L.

    Exclusion Criteria:

  2. Low BMD (BMD absolute value consistent with a T-score≤-2.5 and >-4.0 at either the lumbar spine or total hip). The BMD equivalents by T-score thresholds for each DXA scanner manufacturer are provided below.
  3. Have at least one of the following risk factors:

    1. history of fragility fracture
    2. parental history of hip fracture
    3. low body weight (BMI≤19kg/m2)
    4. elderly (age≥65y)
    5. current smoker
  4. Voluntarily signed written informed consent

Exclusion criteria

  1. Bone/metabolic disease:

    1. Any metabolic bone disease, e.g., osteomalacia or osteogenesis imperfecta,
    2. Paget's disease
    3. Cushing's disease
    4. Hyperprolactinemia
    5. Hypopituitarism
    6. Acromegaly
    7. Current hyperparathyroidism or hypoparathyroidism by medical record.
    8. Current hyperthyroidism or hypothyroidism (allowed if having normal hormone level on thyroid hormone replacement therapy or 5.5μIU/mL<thyroid-stimulating hormone (TSH) level≤10.0μIU/mL, but the serum thyroxine (T4) is within the normal range.
    9. Malabsorption syndrome or any gastrointestinal disorders associated with malabsorption, for example Crohn's Disease and chronic pancreatitis.
    10. Hypocalcemia or hypercalcemia, or serum albumin corrected blood calcium level is not within the normal range of the laboratory;
    11. Vitamin D deficiency: 25 hydroxy vitamin D (25OHD) level <20 ng/mL. (allowed 200,000 units of vitamin D2 injection (trade name: Futai®) once during the screening period, and re-test the 25OHD level once. Those with 25OHD level ≥20 ng/mL can be included
    12. Others such as rheumatoid arthritis, gout, multiple myeloma and so on.
  2. Subjects with a history of greater than 2 vertebral fractures.
  3. Malignancy within the 5 years before enrollment (except fully resected cutaneous basal cell or squamous cell carcinoma, cervical or breast ductal carcinoma in situ).
  4. Severe renal disease, creatinine clearance <30mL/min
  5. Liver or biliary diseases:

    1. Cirrhosis of the liver;
    2. Biliary tract abnormalities (except asymptomatic gallstones);
    3. Positive Hepatitis C virus (HCV) antibody;
    4. Positive hepatitis B surface antigen (HBsAg) test with the peripheral blood hepatitis B virus deoxyribonucleic acid (HBV DNA) titer test ≥1×103 copies/mL (if positive HBsAg with the peripheral blood HBV DNA titer test <1× 103 copies/mL, the subject is eligible for selection if the investigator believes that the subject is in a stable phase of chronic hepatitis B and will not increase the risk of the subject,;
    5. Alkaline phosphatase <lower limit of normal (LLN); alkaline phosphatase or total bilirubin ≥ 1.5 times the upper limit of normal (ULN); serum aspartate aminotransferase (AST) ≥ 2.0×ULN; serum alanine Acid aminotransferase (ALT) ≥2.0×ULN;
  6. Oral/Dental Diseases

    1. Prior history or current evidence of osteomyelitis or osteonecrosis of the jaw.
    2. Active dental or jaw condition which requires oral surgery.
    3. Planned invasive dental procedure.
    4. Non-healed dental or oral surgery.
  7. DXA measurements:

    1. Less than two lumbar vertebrae evaluable for DXA measurements.
    2. Height, weight, or girth that could preclude accurate DXA measurements.
  8. Administration of the following medications:

    1. RANKL inhibitor, fluoride or strontium salt or intravenous bisphosphonate within the past 5 years;
    2. Oral bisphosphonates, allowed if patients had the following conditions :

      • Cumulative use> 3 months but <3 years: ≥ 6 months before the last medication was taken from the screening visit;
      • Cumulative use ≤3 months;
    3. parathyroid hormone (PTH) or parathyroid hormone analogs (PTHa) within 6 weeks before screening, such as teriparatide; anabolic hormones or testosterone; glucocorticoids (equivalent to> 5 mg/day strength Pine> 10 days); systemic hormone replacement therapy; selective estrogen receptor modulators (SERMs), such as raloxifene; tibolone; calcitonin; active vitamin D and its analogs; other bone active drugs including anticonvulsants (except benzodiazepines) and heparin; long-term systemic use of ketoconazole, androgens, corticotropin, cinacalcet, aluminum, lithium, protease inhibitors, methotrexate, Gonadotropin releasing hormone agonist;
  9. Positive human immunodeficiency virus (HIV) antibody.
  10. Self-reported alcohol or drug abuse [defined as drinking an average of 14 units or more of alcoholic beverages per week in the 3 months before screening (1 unit = 350 mL of beer, or 45 mL of liquor, or 150 mL of wine)]
  11. Known allergy to the treatment drugs used in the research protocol, including allergy to the test drugs
  12. Have received any other experimental drug treatment or prior participation in another interventional clinical trial within 3 months before screening
  13. Other severe acute or chronic diseases, psychiatric disorder or abnormal laboratory tests, etc., in the opinion of the investigator, not suitable for participating in this research.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: LY06006 60mg

injection

Interventions:

Drug: LY06006 Injection; Dietary Supplement: Elemental Calcium; Dietary Supplement: Vitamin D

60 mg/1 ml, once every 6 months administered subcutaneously, two injections in total
Andre navn:
  • recombinant human monoclonal anti-RANKL antibody injection
Placebo komparator: Placebo

injection

Interventions:

Drug: Placebo; Dietary Supplement: Elemental Calcium; Dietary Supplement: Vitamin D

60 mg/1 ml, once every 6 months administered subcutaneously, two injections in total
Andre navn:
  • recombinant human monoclonal anti-RANKL antibody injection

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine
Tidsramme: Baseline and Month 12
Percent Change From Baseline in Bone Mineral Density (BMD) at the Lumbar Spine at Month 12
Baseline and Month 12

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine
Tidsramme: Baseline and Month 6
Percent Change From Baseline in BMD at the Lumbar Spine at Month 6
Baseline and Month 6
Percent Changes in total hip BMD
Tidsramme: Baseline,Month 6 and Month 12
Percent Changes in total hip BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Changes in femoral neck BMD
Tidsramme: Baseline,Month 6 and Month 12
Percent Changes in femoral neck BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Changes in trochanteric BMD
Tidsramme: Baseline,Month 6 and Month 12
Percent Changes in trochanteric BMD from baseline at 6 and 12 months of treatment
Baseline,Month 6 and Month 12
Percent Change in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) From Baseline
Tidsramme: Baseline, Month 1, Month 6 and Month 12
Percent Change From Baseline in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) From Baseline at Month 1, Month 6, and Month 12
Baseline, Month 1, Month 6 and Month 12
Percent Change in Serum Procollagen Type I N Propeptideserum (s-PINP) From Baseline
Tidsramme: Baseline, Month 1, Month 6 and Month 12
Percent Change From Baseline in Serum Procollagen Type I N Propeptideserum (s-PINP) From Baseline at Month 1, Month 6, and Month 12
Baseline, Month 1, Month 6 and Month 12

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Zhenlin Zhang, doctor, Shanghai 6th People's Hospital

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

30. juni 2019

Primær fullføring (Forventet)

30. september 2021

Studiet fullført (Forventet)

31. desember 2021

Datoer for studieregistrering

Først innsendt

20. april 2021

Først innsendt som oppfylte QC-kriteriene

17. september 2021

Først lagt ut (Faktiske)

29. september 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. september 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

17. september 2021

Sist bekreftet

1. september 2021

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • LY06006/CT-CHN-302

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

Nei

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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