Early Phase 1 Myeloma Trial, Recruiting NCT07493135 Sponsor: Suzhou Immunofoco Biotechnology Co., Ltd Condition: Myeloma
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Early Phase 1 Myeloma Trial, Recruiting

NCT07493135
Recruiting Early 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:

  • People aged 18 to 80 years (inclusive), of any sex
  • People whose general health and ability to carry out daily activities falls within an acceptable range, as measured by a standard medical scale called the ECOG performance status (scores 0, 1, or 2)
  • People who have been diagnosed with multiple myeloma that has come back or stopped responding to treatment, and who have already received at least 3 previous rounds of treatment — including specific types of therapy known as proteasome inhibitors and immunomodulatory agents
  • People of childbearing potential, and their partners, who agree to use highly effective contraception from the time of signing the consent form until 12 months after the last dose, and who agree not to donate eggs or sperm during that period
  • People who voluntarily sign and date a written consent form agreeing to take part in the study
  • People who are willing and able to follow the study schedule, attend appointments, and complete all required tests and follow-up visits

Who may not be able to join:

  • Women who are pregnant or currently breastfeeding
  • People who have had, or currently have, another type of cancer (in addition to multiple myeloma)
  • People who test positive for HIV; have active hepatitis B virus infection above a certain level; have active or chronic hepatitis C; test positive for syphilis; or have an active cytomegalovirus (CMV) infection
  • People who have an active infection that is not well controlled, based on the treating doctor's assessment
  • People who have uncontrolled fluid build-up around the lungs, heart, or abdomen at the time of enrolment
  • People with a history of severe allergic reactions such as anaphylactic shock; a known severe allergic reaction to the study treatment (IMV102) or any of its ingredients; or a known severe allergic reaction to a medication called tocilizumab
  • People with serious mental health conditions
  • People who have previously had a solid organ transplant (such as a kidney, liver, or heart transplant)
  • People whom the study doctor assesses as unable or unwilling to follow the requirements of the study
  • People with other serious or uncontrolled medical conditions that the study doctor considers would make participation unsafe or unsuitable

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 28 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Phone: 15800706091

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
Early Phase 1
Sponsor
Suzhou Immunofoco Biotechnology Co., Ltd
Registry
ClinicalTrials.gov
Start date
31 March 2026
Est. completion
1 April 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

To evaluate the safety of IMV102 injection in patients with relapsed/refractory multiple myeloma

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: 28 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