Phase 1 Myeloma Trial, Recruiting NCT06270888 Sponsor: University of Chicago Condition: Myeloma
Back to Myeloma

Phase 1 Myeloma Trial, Recruiting

NCT06270888
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older who have been diagnosed with multiple myeloma that has come back or stopped responding to treatment, with up to 5 bone lesions that can be treated with radiation therapy, and whose bone lesions score within a certain safety range for spinal stability (confirm with trial site)
  • People who have already received appropriate standard treatments, as determined by the treating doctor
  • People who have at least one tumour that can be measured and is a suitable size for radiation treatment (roughly between a small grape and a large orange in volume)
  • People who have a certain level of physical functioning, as rated by their doctor using a standard scale (an ECOG performance status of 2 or better) (confirm with trial site)
  • People whose organ function — such as liver and kidney — meets acceptable levels based on blood test results, as confirmed by the study doctor
  • Women of childbearing potential who have a negative pregnancy test taken within 72 hours before starting the study
  • Women of childbearing potential who agree to use effective contraception during treatment and for 5 months after the last dose
  • Men who are sexually active with women of childbearing potential and agree to use effective contraception during treatment and for 7 months after the last dose, and who agree to avoid donating sperm during that time
  • People who are willing and able to attend scheduled visits, follow the treatment plan, and meet all other study requirements
  • People who are able to give their own informed consent by signing a consent form approved by an ethics committee

Who may not be able to join:

  • People whose bone lesion scores on the spinal instability or fracture risk scales fall outside the acceptable safety range for this trial (confirm with trial site)
  • People who are currently receiving any other anti-myeloma or systemic treatment at the same time as the study (concurrent steroids are permitted)
  • People who are still experiencing significant side effects from a previous treatment (generally above a mild level), with some exceptions for nerve-related side effects, hair loss, or recent surgery recovery — confirm details with trial site
  • People who have previously received radiation to the area planned for treatment in this trial (if that prior radiation was less than 10% of the originally prescribed dose) (confirm with trial site)
  • People who have received certain prior chemotherapy within 2 weeks, or certain prior antibody or targeted drug treatments within 7 days, of starting radiation
  • People with another known cancer that could make it difficult to interpret the trial results, unless specifically approved by the lead researcher
  • People with a known history of non-infectious lung inflammation that required steroid treatment
  • People with evidence of a scarring or inflammatory lung disease
  • People with a current seizure disorder
  • People with a known psychiatric condition or substance use disorder that would make it difficult to follow the study requirements
  • Women who are pregnant, breastfeeding, or planning to become pregnant during the trial and up to 120 days after the last dose; men planning to father children during that same period
  • People with known active Hepatitis B or Hepatitis C infection, if liver lesions are being considered for treatment
  • People who have had a heart attack or stroke within the past 6 months, uncontrolled chest pain within the past 3 months, a history of certain serious heart rhythm problems, or other significant heart conditions
  • People who require daily supplemental oxygen due to a heart or cardiovascular condition
  • People currently taking statin medications, unless they have been on a stable dose for more than 3 months before the study and have not shown signs of muscle enzyme elevation (confirm with trial site)
  • People with a current or past history of significant muscle disorders, recent unresolved muscle injury, or any condition known to raise a muscle enzyme called creatine kinase (CK)
  • People who are currently imprisoned or held in a detention facility
  • People who are under a legal order requiring them to receive psychiatric or medical treatment

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Yasmin Hasan, MD, University of Chicago

Phone: (773) 702-2856

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
8 September 2025
Est. completion
1 May 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Maximum Tolerated Dose of Radiation of Per Fraction

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov