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RecruitingNCT07825454AIMSSUpdated Nov 10, 2026

Pilot Study of Hydroxychloroquine for the Treatment of AIMSS

A Phase 2 interventional study of Hydroxychloroquine Sulfate (HCQ) in Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS), Joint Pain and Breast Cancer, sponsored by Indiana University. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Indiana University · Phase 2, Interventional, and Treatment

Updated Nov 10, 2026Now RecruitingSite recruiting status changed+1 moreGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS)
  • Joint Pain
  • Breast Cancer

Keywords

  • Hydroxychloroquine
  • Joint Pain
  • Aromatase Inhibitor Associated Musculoskeletal Symptoms (AMISS)
03

In context

Arthralgia

277 studies on the registry are indexed under Arthralgia; 54 are open to participants now.

This study's planned enrollment of 35 is below the median of 73 across 218 interventional studies indexed under Arthralgia.

Browse Arthralgia studies →

Lead sponsor

Indiana University is the lead sponsor of 986 studies on the registry; 198 are open to participants now.

Of its 148 completed or terminated interventional studies of FDA-regulated products, 118 (80%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age ≥ 18 years at the time of
  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 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. PS 0-2
  8. Adequate organ function:

    1. ≥1,500/µL
    2. ≥11.0 g/dL
    3. count ≥100,000/µL
    4. Serum creatinine ≤1.5× (ULN) or ≥60 mL/min/1.73m2
    5. Total ≤1.5× ULN (except in patients with documented Gilbert's disease, who must have a total bilirubin \< 3.0 mg/dL)
    6. 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

Exclusion Criteria:

  1. Current or prior use of hydroxychloroquine or chloroquine within 6 months
  2. Known 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 class)
  5. prolongation (>450 msec) at screening or history of significant arrhythmias requiring treatment
  6. Moderate to severe renal impairment ( \<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 defined as: cortisone >50mg; hydrocortisone >40mg, prednisone >10mg, methylprednisolone >8mg or dexamethasone >1.5mg; or another agent Note: Topical or inhaled corticosteroids are allowed
  15. Other active 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
Terms in these criteria, in plain language(16)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (estimated)

Study arms

  • Experimental
    Hydroxychloroquine sulfate

    Hydroxychloroquine sulfate, 400 mg orally once daily

    Drug: Hydroxychloroquine Sulfate (HCQ)

Interventions

06

What researchers measure

Primary outcomes

  1. To evaluate the efficacy of hydroxychloroquine

    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).

    Time frame: Day 1 and Week 12

Secondary outcomes

  1. Proportion of patients achieving a clinically meaningful improvement

    To assess the proportion of patients achieving a clinically meaningful improvement (≥2-point reduction) in BPI Average Pain score.

    Time frame: Day 1 and Week 12

  2. Changes in BPI Worst Pain and Pain Interference scores

    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).

    Time frame: Day 1 and Week 12

  3. Changes in endocrine therapy related quality of life

    To assess changes in endocrine therapy related quality of life by FACT-ES (5 point Likert-type scale).

    Time frame: Day 1 and Week 12

  4. Changes in grip strength

    To assess changes in grip strength as an objective measure of function using Jamar hand dynamometers (scale of 0-200lbs).

    Time frame: Day 1 and Week 12

  5. Patient-reported global impression of change

    To evaluate patient-reported global impression of change using the Patient Global Impression of Change (PGIC) (scale 0-6, 6 being the worst outcome).

    Time frame: Week 12

  6. Safety of hydroxychloroquine in this patient population

    To assess safety of hydroxychloroquine in this patient population using NCI CTCAE v5.0 (grade 1-5, 5 being the worst outcome).

    Time frame: Day 1, Week 4, Week 12, 30 days post EOT

  7. Tolerability of hydroxychloroquine in this patient population

    To assess tolerability of hydroxychloroquine in this patient population via number of patients who completed treatment.

    Time frame: Day 1, Week 4, Week 12, 30 days post EOT

  8. Adherence to aromatase inhibitor therapy

    To evaluate adherence to aromatase inhibitor therapy during the study period via number of patients who completed treatment based on self-report.

    Time frame: Screening, Day 1, and Week 12

07

Study locations

1 of 1 sites recruiting
  • Indiana University Melvin and Bren Simon Comprehensive Cancer Center
    Indianapolis, Indiana 46202, United States
    Recruiting
    • Niraj Shah, MS · Contactshahnir@iu.edu · 317-278-3420
    • Tarah Ballinger, MD · Principal investigator
08

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Nov 10, 2026
Sites
Indiana University Melvin and Bren Simon Comprehensive Cancer Center is now Recruiting
Nov 10, 2026
Start date
Sep 2026→Oct 19, 2026 (actual)
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Not yet recruiting→Recruiting
    Indiana University Melvin and Bren Simon Comprehensive Cancer Center is now Recruiting
    Start date Sep 2026→Oct 19, 2026 (now actual)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07825454
Lead sponsor
Indiana University
Collaborators
100 Voices of Hope
Responsible party
Tarah J Ballinger, MD (Associate Professor, Indiana University) — Principal investigator
First posted
Sep 17, 2026
Start date
Oct 19, 2026
Primary completion
Dec 2029 (estimated)
Completion
Dec 2029 (estimated)
Last update
Nov 10, 2026

Study contacts

Niraj Shah, MS
Contact
shahnir@iu.edu
317-278-3420
Tarah Ballinger, MD
principal investigator · IUSCCC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Hydroxychloroquine

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