Phase 2 Myeloma Trial, Recruiting NCT05908409 Sponsor: IDP Discovery Pharma S.L. Condition: Myeloma
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Phase 2 Myeloma Trial, Recruiting

NCT05908409
Recruiting Phase 2

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.

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 2: approximately ~30% 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: 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

Status
Recruiting
Phase
Phase 2
Sponsor
IDP Discovery Pharma S.L.
Registry
ClinicalTrials.gov
Start date
5 June 2023
Est. completion
22 December 2025

Where this trial is recruiting

🇪🇸 Spain

Primary endpoints

Phase 1: Dose Escalation; Phase 1: Dose Escalation; Phase 2: Expansion Phase

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