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Segurança e Eficácia do PTH-IA

16 de outubro de 2026 atualizado por: National Institute of Dental and Craniofacial Research (NIDCR)

Um Estudo de Segurança e Eficácia de Primeira Administração em Seres Humanos, Aberto, de Fase 1/2, com Escalonamento de Dose, Avaliando a Administração Subcutânea de PTH-IA em Adultos e Crianças com Condrodisplasia Metafisária de Jansen (JMC)

Jansen s Metaphyseal Chondrodysplasia (JMC) is a very rare disorder with only approximately 30 people known to have the disease worldwide. It is caused by parathyroid hormone 1 receptor (PTH1R) variants leading to constitutive activation of the receptor for parathyroid hormone (PTH) and parathyroid hormone-related peptide (PTHrP). PTH1R is predominantly expressed in the kidneys and bone and growth-plate chondrocytes. Individuals with JMC develop severe growth impairment resulting in significant short stature, scoliosis, frequent fractures, bone pain, mineral-ion abnormalities (typically hypercalcemia and hypercalciuria), hypertension, and chronic kidney disease due to nephrocalcinosis and nephrolithiasis. Children often undergo multiple surgeries for skeletal fractures and deformities; mobility is commonly impaired, usually requiring assistive devices for ambulation. Other complications may include premature closure of cranial sutures and cranial nerve compressions with the potential for vision and/or hearing loss [1-3]. Physical function impairment and the need for complication-related operations have profound deleterious effects on quality of life in individuals with JMC. There are currently no approved therapies for JMC, and novel therapies are critically needed to prevent irreversible disease complications and improve patient quality of life.

The inventors of the drug, parathyroid hormone inverse agonist (PTH-IA), have considerable expertise in both the basic and clinical aspects of PTH/PTHrP receptor molecular biology and pharmacology. They reported the first PTH1R JMC mutations (including the H223R mutation) over 20 years ago and identified certain PTH antagonist ligands that function as inverse agonists on the PTH1R JMC mutant receptors [2, 4]. These ligands suppress the mutant receptor s elevated basal rates of cAMP signalling, as assessed in cultured cells and animal models. In vivo studies confirm that inverse agonist ligands may be effective in treating JMC. This study involves the use of PTH-IA, a 30-amino acid PTH inverse agonist ligand with the amino acid sequence [Leu11,dTrp12,Trp23,Tyr36]-PTHrP(7-36)NH2. We hypothesize that PTH-IA will be a safe and effective treatment for individuals with JMC.

Visão geral do estudo

Status

Recrutamento

Condições

Intervenção / Tratamento

Descrição detalhada

Study Description:

This is a Phase 1/2 open-label, single-arm study to evaluate the safety of multiple ascending doses of PTH-IA administered subcutaneously twice a day in individuals with JMC conducted at the National Institutes of Health Clinical Center.

Objectives Primary Objectives

Period 1 - Adult

  1. Evaluate the safety and tolerability of PTH-IA in adults with JMC (>=18 years)
  2. Evaluate the pharmacokinetics (PK) of multiple ascending doses of PTH-IA in adults (>= 18 y/o) years old with JMC

Period 2 - Adult and Pediatrics

  1. Evaluate the safety and tolerability of PTH-IA in adults and children aged 3-17 years old with JMC
  2. Evaluate the pharmacokinetics (PK) of multiple ascending doses of PTH-IA in children aged 3-17 years old with JMC
  3. Evaluate the effect of PTH-IA on serum PTH levels on children and adults with JMC

Secondary Objectives

Periods 1 and 2

  1. Identify the optimal dose range of PTH-IA
  2. Evaluate potential measures of efficacy of PTH-IA in JMC

Exploratory Objectives

Periods 1 and 2

  1. Evaluate the effect of PTH-IA on physical function
  2. Evaluate the effect of PTH-IA on pain and health-related quality of life (QOL)
  3. Evaluate the immunogenicity of PTH-IA
  4. Describe the baseline and response to treatment histological characteristics of bone lesions in JMC

Endpoints Primary Endpoints

Period 1

  1. Dose limiting toxicities (DLTs) and incidence, severity, seriousness, and causality of all treatment-emergent adverse events (TEAEs)
  2. PK parameters after multiple ascending doses of PTH-IA

Period 2

  1. Dose limiting toxicities (DLTs) and incidence, severity, seriousness, and causality of all treatment-emergent adverse events (TEAEs)
  2. PK parameters after multiple ascending doses of PTH-IA
  3. Change in serum PTH from baseline to end of treatment

Secondary Endpoints

Periods 1 and 2

  1. Absolute levels and percentage change from baseline in serum corrected calcium pre- and post-intervention at end of treatment
  2. Absolute levels and change in ratio of serum corrected calcium to PTH ([mg/dl]/[pg/ml]) pre- and post-intervention at end of study
  3. Absolute levels and percentage change from baseline in fractional excretion of calcium at end of treatment
  4. Change in tubular reabsorption of phosphate and ratio of tubular maximum reabsorption of phosphate to GFR between pre- and post-intervention at end of treatment
  5. Absolute levels and percentage change from baseline in urine nephrogenous cAMP at end of treatment
  6. Absolute levels and percentage change from baseline in serum phosphate at end of treatment
  7. Change in bone turnover markers (P1NP, BSALP, CTX, osteocalcin) between pre- and post-intervention at end of treatment
  8. Absolute levels and percentage change from baseline in markers of mineral homeostasis: 1,25(OH)2 vitamin D and ratio of 1,25(OH)2 vitamin D to PTH at end of treatment
  9. Change in pre-defined sentinel skeletal lesion metabolic activity representing region of most intense pathology as measured by 18F- NaF PET/CT (<= 5 lesions) between pre- and post-intervention at end of treatment
  10. Change in pre-defined target skeletal lesion mineral density representing region of most intense pathology as measured by 18F- NaF PET/CT (<= 5 lesions) between pre- and postintervention at end of treatment
  11. Change in nephrocalcinosis scores on ultrasound from baseline to end of treatment (0-no nephrocalcinosis and 3- severe nephrocalcinosis)
  12. Change in HR-pQCT parameters of the radius and tibia: total BMD, cortical and trabecular BMD; cortical thickness, cortical porosity, BV/TV, trabecular number, thickness, and separation; stiffness and failure load of the peripheral skeleton
  13. Minimally effective dose defined by dose at which the mean of two highest PTH levels increases to 30-40 pg/mL (in individuals with baseline PTH <= 20 pg/mL) in the absence of DLTs. In individuals with baseline PTH >20 pg/mL, the optimal dose will be the dose at which the mean of two highest PTH obtained increases to 55-65 pg/mL in the absence ofDLTs.

Exploratory Endpoints

Periods 1 and 2

  1. Change from baseline in range of motion of upper and lower extremities
  2. Change from baseline in manual muscle strength testing of bilateral upper and lower extremities
  3. Change from baseline in gait assessment
  4. Change from baseline in assessment of skeletal bowing
  5. Change from baseline in walking speed
  6. Change from baseline in PROMIS pain intensity, pain interference, mobility, and fatigue scores
  7. Development and characterization of anti-drug antibodies (ADAs)
  8. JMC lesion histology as assessed by bone biopsies

Tipo de estudo

Intervencional

Inscrição (Estimado)

12

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

  • Estados Unidos
    • Maryland
      • Bethesda, Maryland, Estados Unidos, 20892
        • Recrutamento
        • National Institutes of Health Clinical Center
        • Contato:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Número de telefone: TTY dial 711 800-411-1222
          • E-mail: ccopr@nih.gov

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

3 anos a 100 anos (Filho, Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

  • INCLUSION CRITERIA:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  1. Willingness of participant and/or guardian to sign a written informed consent form, which must be obtained prior to initiation of study procedures.

  2. Period 1: Adults >=18 years of age

    Period 2: Adults and children 3-17 years of age

  3. Minimum body weight of 35 kg for participation in Period 1 and 18 kg for participation in Period 2.

  4. Have an activating germline mutation of PTHIR (H223R, I458K, I458R, T410P, or T410R)

  5. Female participants of reproductive potential must agree to use one form of highly effective contraception. Highly effective contraception includes:

    Total abstinence (when this is in line with the preferred and usual lifestyle of the participant). Periodic abstinence (e.g. calendar, ovulation, symptothermal, post- ovulation methods) and withdrawal are not acceptable methods of contraception.

    Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment.

    Male sterilization (at least 6 months prior to screening). For female participants in the study, the vasectomized male partner should be the sole partner for that participant for the study duration.

    Use of oral, injected, or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate <1%), for example hormonal vaginal ring or transdermal hormone contraception

    Placement of an intrauterine device (IUD) or intrauterine system (IUS)

    Barrier methods of contraception used correctly by the male partner: condom or occlusive cap (diaphragm or cervical/ vault caps) with spermicidal foam/gel/film/cream/vaginal suppository.

  6. For males of reproductive potential: use of condoms or other methods described above to ensure effective contraception with partner.

  7. Stated willingness to comply with all study procedures and availability for the duration of the study, including the ability and willingness to travel to the NIH Clinical Center.

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

  1. Pregnancy or lactation
  2. 25-hydroxyvitamin D <=20 ng/mL. Patients will be eligible for rescreening after a repletion period lasting up to 6 months.
  3. Clinically significant renal disease with estimated glomerular filtration rate (eGFR) <=45 mL/ min/1.73 m2.
  4. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >2 times the upper limit of normal. If transaminitis is present, patients will be eligible for rescreening for a period of up to 6 months.
  5. Hgb <12 gm/dL for women and girls >=16 years, <=13 gm/dL for men and boys >=16 years, and <=11.5 gm/dL in children <=15 years. If reduced hemoglobin levels are related to iron, B12, or folate deficiency, patients will be eligible for rescreening after a repletion period lasting up to 6 months.
  6. Hypersensitivity or intolerance to any active substance or excipient of PTH-IA
  7. History of surgical removal of all parathyroid glands.
  8. Treatment with bisphosphonate use within 6 months of screening
  9. Treatment with denosumab within 3 months of screening
  10. Treatment with thiazides within 4 weeks of screening
  11. Any other significant medical conditions that, in the opinion of the study team, may present a concern for participant safety or difficulty with data interpretation.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Treatment with PTH-IA

All participants will receive PTH-IA for up to 90+/-7 days in Period 1, and 24 weeks +/- 7 days in Period 2.
Medicamento: PTH-IA

PTH-IA is a 30-amino acid peptide expected to act as an inverse agonist, decreasing the proportion of mutant PTH1R receptors in the active-state conformation and leading to a reduction in basal cAMP signaling. This hypothesis is based on results from PTH-IA treatment of cells and animal models expressing the different PTH1R mutations seen in JMC individuals. In-vitro studies of HEK293 cells stably transfected with a Glosensor cAMP reporter and plasmids expressing the different PTH1R constitutively active mutant JMC alleles (H223R, I458K, I458R, T410P, and T410R) showed that the cells displayed agonist-independent cAMP generation. Treatment of cells expressing the different PTH1R mutations with PTH-IA resulted in a rapid and persistent reduction in basal cAMP signaling, indicating that the peptide can act as an inverse agonist and thus decreases the proportion of mutant receptors in the active-state conformation.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Period 1 - Adult: Evaluate the safety and tolerability of PTH-IA in adults with JMC (>= 18 years)
Prazo: 104 +/- 10 days

To assess dose-limiting toxicities (DLTs) and incidence, severity, seriousness, and causality of all treatment-emergent adverse events (TEAEs).
104 +/- 10 days
Period 1 - Adult: Evaluate the pharmacokinetics (PK) of multiple ascending doses of PTH-IA in adults (>= 18 y/o) years old with JMC
Prazo: 104 +/- 10 days

To determine PK parameters after multiple ascending doses of PTH-IA.
104 +/- 10 days
Period 2 - Adult and Pediatrics: Evaluate the safety and tolerability of PTH-IA in adults and children aged 3-17 years old with JMC.
Prazo: 28 weeks +/- 10 days

To assess dose-limiting toxicities (DLTs) and incidence, severity, seriousness, and causality of all treatment-emergent adverse events (TEAEs).
28 weeks +/- 10 days
Period 2 - Adult and Pediatrics: Evaluate the pharmacokinetics (PK) of multiple ascending doses of PTH-IA in children aged 3-17 years old with JMC.
Prazo: 28 weeks +/- 10 days

To determine PK parameters after multiple ascending doses of PTH-IA.
28 weeks +/- 10 days
Period 2 - Adult and Pediatrics: Evaluate the effect of PTH-IA on serum PTH levels in children and adults with JMC.
Prazo: 28 weeks +/- 10 days

To evaluate changes in serum PTH from baseline to the end of treatment.
28 weeks +/- 10 days

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Periods 1 and 2 - Identify the optimal dose range of PTH-IA.
Prazo: Period 1: 104 +/- 10 days. Period 2: 28 weeks +/- 10 days.

To measure the absolute levels and percentage change: - From baseline in serum-corrected calcium pre- and post-intervention at the end of treatment.- In the ratio of serum-corrected calcium to PTH ([mg/dl]/[pg/ml]) pre- and post-intervention at the end of the study.- From baseline in fractional excretion of calcium at the end of treatment.- From baseline in urine nephrogenous cAMP at the end of treatment.- From baseline in serum phosphate at the end of treatment.- From baseline in markers of mineral homeostasis: 1,25(OH)2 vitamin D and ratio of 1,25(OH)2 vitamin D to PTH at the end of treatment.- To define the minimally effective dose defined by the dose at which the mean of the two highest PTH levels increases to 30-40 pg/mL (in individuals with baseline PTH <= 20 pg/mL) in the absence of DLTs.
Period 1: 104 +/- 10 days. Period 2: 28 weeks +/- 10 days.
Periods 1 and 2 - Evaluate potential measures of efficacy of PTH-IA in JMC.
Prazo: Period 1: 104 +/- 10 days. Period 2: 28 weeks +/- 10 days.

To measure the change in: - Tubular reabsorption of phosphate and the ratio of tubular maximum reabsorption of phosphate to GFR between pre- &amp; post-intervention at the end of treatment.- Bone turnover markers (P1NP, BSALP, CTX, osteocalcin) between pre- &amp; post-intervention.- Pre-defined sentinel skeletal lesion metabolic activity representing region of most intense pathology as measured by 18F- NaF PET/CT (<= 5 lesions) between pre- &amp; post-intervention.- Pre-defined target skeletal lesion mineral density representing region of most intense pathology as measured by 18F- NaF PET/CT (<= 5 lesions) between pre- &amp; post-intervention. - Nephrocalcinosis scores on ultrasound from baseline to end of treatment (0-no nephrocalcinosis to 3-severe).- HR-pQCT parameters of the radius and tibia: total BMD, cortical and trabecular BMD; cortical thickness, cortical porosity, BV/TV, trabecular number, thickness, and separation; stiffness and failure load of the peripheral skeleton.
Period 1: 104 +/- 10 days. Period 2: 28 weeks +/- 10 days.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

National Institute of Dental and Craniofacial Research (NIDCR)

Investigadores

  • Investigador principal: Alison M Boyce, M.D., National Institute of Dental and Craniofacial Research (NIDCR)

Publicações e links úteis

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Links úteis

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

27 de maio de 2026

Conclusão Primária (Estimado)

1 de junho de 2029

Conclusão do estudo (Estimado)

1 de junho de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

18 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

18 de abril de 2026

Primeira postagem (Real)

21 de abril de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de outubro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

16 de outubro de 2026

Última verificação

5 de outubro de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • 10001653
  • 001653-D

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

This study will comply with the NIH Data Sharing Policy and the Clinical Trials Registration and Results Information Submission rule.

Prazo de Compartilhamento de IPD

Results from this trial will be made available 12 months after the primary study completion date.

Critérios de acesso de compartilhamento IPD

PI will consider reasonable requests from qualified researchers for access to clinical data.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • CSR

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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