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Pilot Study of Hydroxychloroquine for the Treatment of AIMSS (AIMSS)

16 de septiembre de 2026 actualizado por: Tarah J Ballinger, MD, Indiana University

A Phase II Single-Arm Pilot Study of Hydroxychloroquine for the Treatment of Aromatase Inhibitor-Associated Musculoskeletal Syndrome

The purpose of this study is to evaluate the effectiveness of hydroxychloroquine sulfate (a type of drug commonly used to treat joint pain caused by inflammation, swelling) in reducing joint pain associated with Aromatase Inhibitor Associated Musculoskeletal Syndrome (AIMSS) for patients with breast cancer.

Descripción general del estudio

Descripción detallada

Aromatase Inhibitor (AI) therapy is highly effective for post-menopausal, estrogen receptor (ER) positive breast cancer, yet the clinical effectiveness of AI therapy is limited by noncompliance and early treatment discontinuation due to musculoskeletal side effects, which include joint pain, joint stiffness, bone pain, muscle weakness, and myalgias. Methods to improve compliance to AI therapy have the potential to increase survival.

This study will look at hydroxychloroquine (HCQ), a disease-modifying antirheumatic drug (DMARD) with well-established anti-inflammatory and immunomodulatory properties. It is FDA-approved for the treatment of conditions characterized by chronic inflammatory joint pain similar to AIMSS. This single-arm, proof of concept study will look for an improvement in joint pain for patients undergoing standard of care treatment involving AI therapy.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

35

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Niraj Shah, MS
  • Número de teléfono: 317-278-3420
  • Correo electrónico: shahnir@iu.edu

Ubicaciones de estudio

    • Indiana
      • Indianapolis, Indiana, Estados Unidos, 46202
        • Indiana University Melvin and Bren Simon Comprehensive Cancer Center
        • Investigador principal:
          • Tarah Ballinger, MD
        • Contacto:
          • Niraj Shah, MS
          • Número de teléfono: 317-278-3420
          • Correo electrónico: shahnir@iu.edu

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Age ≥ 18 years at the time of informed consent
  2. Ability to provide written informed consent and HIPAA authorization
  3. Diagnosis of DCIS or stage I, II, or III breast cancer
  4. Currently receiving adjuvant aromatase inhibitor therapy (anastrozole, letrozole or exemestane) for ≥ 4 weeks prior to enrollment Note: Concurrent use of ovarian suppression is allowed Note: Concurrent use of CDK4/6 inhibitors is not allowed due to cytopenia risk
  5. New or worsening self-reported musculoskeletal pain that began or significantly worsened after initiation of AI therapy
  6. BPI average pain score of ≥ 4 during screening
  7. ECOG PS 0-2
  8. Adequate organ function:

    1. Absolute neutrophil count ≥1,500/µL
    2. Hemoglobin ≥11.0 g/dL
    3. Platelet count ≥100,000/µL
    4. Serum creatinine ≤1.5× upper limit of normal (ULN) or eGFR ≥60 mL/min/1.73m2
    5. Total bilirubin ≤1.5× ULN (except in patients with documented Gilbert's disease, who must have a total bilirubin < 3.0 mg/dL)
    6. AST and ALT ≤1.5× ULN
  9. Must agree to maintain stable doses of any analgesic medications or other AIMSS related therapies during the study period Note: rescue doses of acetaminophen or ibuprofen allowed on a non-daily basis, unless not new

Exclusion Criteria:

  1. Current or prior use of hydroxychloroquine or chloroquine within 6 months
  2. Known hypersensitivity to hydroxychloroquine, chloroquine, or 4-aminoquinoline compounds
  3. History of retinopathy or retinal vein occlusion issues Note: While there is an association between retinopathy and HCQ use, this occurs rarely and with long term use with higher cumulative doses that used here. Other clinical trials have not required retinal exam (example: CTO-TBCRC04627, approved by IU IRB)
  4. History of congestive heart failure (any NYHA class)
  5. QTc prolongation (>450 msec) at screening or history of significant arrhythmias requiring treatment
  6. Moderate to severe renal impairment (eGFR <60 mL/min/1.73m2)
  7. Use of a prohibited concomitant medication (refer to Section 6.3.2) that cannot be discontinued or changed to an alternate therapy
  8. Known glucose-6-phosphate dehydrogenase (G6PD) deficiency
  9. History of porphyria
  10. History of psoriasis
  11. History of antiepileptic medications
  12. Known history of inflammatory arthritis (example: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis) or connective tissue disease (example: systemic lupus erythematosus, scleroderma, polymyositis)
  13. Recent initiation or dose change (within 4 weeks) of medications for pain management (NSAIDs, duloxetine, gabapentin, pregabalin, opioids) Note: Patients on stable doses for >4 weeks are eligible
  14. Patients currently receiving or planned to receive high dose systemic treatment with corticosteroids defined as: cortisone >50mg; hydrocortisone >40mg, prednisone >10mg, methylprednisolone >8mg or dexamethasone >1.5mg; or another immunosuppressive agent Note: Topical or inhaled corticosteroids are allowed
  15. Other active malignancy other than breast cancer requiring systemic therapy
  16. Pregnant or lactating
  17. Co-enrollment in another clinical trial Note: Patients may co-enroll in other clinical trial(s) if the trial(s) does not interfere with the objectives of this trial
  18. Significant psychiatric illness, in the opinion of the investigator, that would limit compliance with study requirements
  19. Any active suicidality or history of active suicidal ideation/behavior/attempt within 1 year prior to screening
  20. Any other condition that, in the opinion of the investigator, would make the patient unsuitable for study participation

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Hydroxychloroquine sulfate
Hydroxychloroquine sulfate, 400 mg orally once daily
Drug: Hydroxychloroquine sulfate Dose: 400 mg orally once daily Duration: 12 weeks

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
To evaluate the efficacy of hydroxychloroquine
Periodo de tiempo: Day 1 and Week 12
To evaluate the efficacy of hydroxychloroquine 400 mg daily in reducing joint pain associated with AIMSS as measured by change in Brief Pain Inventory (BPI) Average Pain score (scored from 0-10; a minimally important difference is a 2-point reduction or 30% from baseline).
Day 1 and Week 12

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of patients achieving a clinically meaningful improvement
Periodo de tiempo: Day 1 and Week 12
To assess the proportion of patients achieving a clinically meaningful improvement (≥2-point reduction) in BPI Average Pain score.
Day 1 and Week 12
Changes in BPI Worst Pain and Pain Interference scores
Periodo de tiempo: Day 1 and Week 12
To evaluate changes in BPI Worst Pain and Pain Interference scores (scored from 0-10; a minimally important difference is a 2-point reduction or 30% from baseline).
Day 1 and Week 12
Changes in endocrine therapy related quality of life
Periodo de tiempo: Day 1 and Week 12
To assess changes in endocrine therapy related quality of life by FACT-ES (5 point Likert-type scale).
Day 1 and Week 12
Changes in grip strength
Periodo de tiempo: Day 1 and Week 12
To assess changes in grip strength as an objective measure of function using Jamar hand dynamometers (scale of 0-200lbs).
Day 1 and Week 12
Patient-reported global impression of change
Periodo de tiempo: Week 12
To evaluate patient-reported global impression of change using the Patient Global Impression of Change (PGIC) (scale 0-6, 6 being the worst outcome).
Week 12
Safety of hydroxychloroquine in this patient population
Periodo de tiempo: Day 1, Week 4, Week 12, 30 days post EOT
To assess safety of hydroxychloroquine in this patient population using NCI CTCAE v5.0 (grade 1-5, 5 being the worst outcome).
Day 1, Week 4, Week 12, 30 days post EOT
Tolerability of hydroxychloroquine in this patient population
Periodo de tiempo: Day 1, Week 4, Week 12, 30 days post EOT
To assess tolerability of hydroxychloroquine in this patient population via number of patients who completed treatment.
Day 1, Week 4, Week 12, 30 days post EOT
Adherence to aromatase inhibitor therapy
Periodo de tiempo: Screening, Day 1, and Week 12
To evaluate adherence to aromatase inhibitor therapy during the study period via number of patients who completed treatment based on self-report.
Screening, Day 1, and Week 12

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Tarah Ballinger, MD, IUSCCC

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2029

Finalización del estudio (Estimado)

1 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

25 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de septiembre de 2026

Publicado por primera vez (Actual)

17 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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