Phase 1 Myeloma Trial, Recruiting NCT06896916 Sponsor: AbbVie Condition: Myeloma
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Phase 1 Myeloma Trial, Recruiting

NCT06896916
Recruiting Phase 1 🇦🇺 Australian site

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:

  • You are generally able to carry out daily activities and care for yourself, with little or no limitation due to your illness (this is measured by a standard scale called ECOG, with a score of 0 or 1)
  • You have been diagnosed with multiple myeloma that has come back or stopped responding to your most recent treatment
  • Your disease can be detected and measured through specific blood, urine, or other laboratory tests

Who may not be able to join:

  • You have previously been treated with a drug called etentamig
  • You have previously received any treatment that targets a protein called BCMA (confirm with trial site for specific therapies this includes)
  • You have previously been treated with either of two specific drugs called iberdomide or mezigdomide (which belong to a class of drugs known as CELMoDs)

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
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: ABBVIE INC., AbbVie

Phone: 844-663-3742

Australian sites

Blacktown Hospital /ID# 265983, Blacktown, New South Wales
Wollongong Hospital /ID# 265625, Wollongong, New South Wales
The Alfred Hospital /ID# 265981, Melbourne, Victoria
Austin Hospital /ID# 265984, Melbourne, Victoria
Sir Charles Gairdner Hospital /ID# 265985, Nedlands, Western Australia

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
Sponsor
Registry
ClinicalTrials.gov
Start date
7 August 2025
Est. completion
1 March 2036

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇫🇷 France 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇴 Norway 🇺🇸 United States

5 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Phase 1: Dose-Limiting Toxicities (DLT)s of Etentamig when given in Combination with Iberdomide in Participants with Relapsed/Refractory Multiple Myeloma (RRMM); Number of Participants with Adverse Events (AE)s

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