Phase 2 Myeloma Trial, Recruiting
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:
- People aged 18 or older
- People whose general health and ability to carry out daily activities meets a certain minimum level, as assessed by their doctor (confirm with trial site)
- People with a life expectancy of at least 3 months
- People who are willing and able to follow the study requirements, in their doctor's opinion
- People who have given written consent to participate, understanding they may withdraw at any time without it affecting their future care
- People diagnosed with chronic lymphocytic leukaemia (CLL), B-cell lymphomas, or multiple myeloma (MM), who are not eligible to receive the currently available treatments for their condition
- People whose blood counts and organ function results meet specific minimum levels — including red blood cells, platelets, white blood cells, liver function, and kidney function — without having needed certain medical support in the 7 days before testing (confirm with trial site for exact values)
- People whose heart pumping function, as measured by an ultrasound of the heart, meets a minimum threshold set by the trial or the treating hospital
Who may not be able to join:
- People who still have significant ongoing side effects from previous treatments (note: hair loss and mild nerve-related symptoms may be acceptable — confirm with trial site)
- Women who are pregnant or breastfeeding
- People of reproductive potential who are not using an effective form of contraception as specified by the trial (confirm with trial site for the full list of accepted methods)
- People with a history of another cancer in the past five years, except for certain minor skin cancers or non-invasive cancers (confirm with trial site)
- People with a history of clinically significant low blood pressure
- People with a history of clinically significant allergic or hypersensitivity reactions
- People with a known history of significant blood vessel disease or a high risk of blood vessel problems — including blood clots, peripheral arterial disease, or inflammation of the blood vessels — as assessed by their treating doctor
- People with a history of heart failure, chest pain (angina), or a heart attack within the past 12 months
- People with high blood pressure or heart rhythm problems that are not well controlled (for example, requiring a medication change in the past 3 months or a hospital admission in the past 6 months)
- People with a history of significant neurological or psychiatric disorders
- People with a clinically significant or active infection
- People with significant non-cancerous liver disease, such as cirrhosis or chronic active hepatitis
- People who are HIV-positive, unless they are on antiviral therapy with very low virus levels; people with active Hepatitis B or C infection, unless successfully treated with undetectable virus levels; or people with an active CMV infection
- People who have received other cancer treatments within 14 days before the start of the trial
- People who have had an organ or stem cell transplant from a donor within the past 3 months, or who currently have graft-versus-host disease (a complication of transplants) requiring immune-suppressing medication
- People who are unable to follow the treatment or follow-up schedule required by the trial
- People who have received a COVID-19 vaccine within 72 hours before starting the study treatment (vaccination should occur either more than 72 hours before starting, or after a specific early study period has ended — confirm with trial site)
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.
Contact this trial
Principal Investigator: Enrique Ocio San Miguel, MD, PhD, Hospital Universitario Marqués de Valdecilla
Phone: +34669616086
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
Where this trial is recruiting
Primary endpoints
Phase 1: Dose Escalation; Phase 1: Dose Escalation; Phase 2: Expansion Phase
Can't join this trial?
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.