๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-03-26

Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutaneous (SC) Injection in Adult Participants With Relapsed or Refractory Multiple Myeloma (NCT06223516)

A Multicenter, Phase 1b, Open-label Study of Etentamig (ABBV-383) Administered Subcutaneously in Subjects With Relapsed or Refractory Multiple Myeloma

๐Ÿ”ต Active, Not Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: AbbVie

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

Multiple myeloma (MM) is a cancer of the blood's plasma cells. The cancer is typically found in the bones and bone marrow (the spongy tissue inside of the bones) and can cause bone pain, fractures, infections, weaker bones, and kidney failure. Treatments are available, but MM can come back (relapsed) or may not get better (refractory) with treatment. This is a study to determine the safety and pharmacokinetics of Etentamig (ABBV-383) in adult participants with relapsed/refractory (R/R) MM. Etentamig (ABBV-383) is an investigational drug being developed for the treatment of R/R MM. This study is broken into 3 Arms: Arm A with 2 parts and Arm B as an expansion. Participants will receive ABBV-383 as a subcutaneous (SC) injection and intravenous (IV) infusion in Arm A and SC injections of ABBV-383 in Arm B. Around 55 adult participants with relapsed/refractory multiple myeloma will be enrolled at approximately 15 sites across the world In Arm A participants will receive one of two doses of Etentamig (ABBV-383) as an SC injection and (IV) infusions, during the 151 week study duration. In Arm B, participants will receive the selected dose from Arm A as SC injections, during the 151 week study duration. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and questionnaires.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Arizona /ID# 260799 โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (15 Sites)

  • Mayo Clinic Arizona /ID# 260799 โ€” Phoenix, Arizona
  • Mayo Clinic Hospital Jacksonville /ID# 262808 โ€” Jacksonville, Florida
  • Sylvester Comprehensive Cancer Center /ID# 260798 โ€” Miami, Florida
  • University of Michigan Comprehensive Cancer Center Michigan Medicine /ID# 261050 โ€” Ann Arbor, Michigan
  • Mayo Clinic - Rochester /ID# 262807 โ€” Rochester, Minnesota
  • Atrium Health Wake Forest Baptist Medical Center /ID# 260807 โ€” Winston-Salem, North Carolina
  • Wisconsin Medical Center /ID# 261085 โ€” Milwaukee, Wisconsin
  • Universitaetsklinikum Frankfurt /ID# 260442 โ€” Frankfurt am Main, Hesse
  • Universitaetsklinikum Koeln /ID# 260445 โ€” Cologne, North Rhine-Westphalia
  • Universitaetsklinikum Hamburg-Eppendorf /ID# 260444 โ€” Hamburg,
  • Hadassah Medical Center-Hebrew University /ID# 261446 โ€” Jerusalem, Jerusalem
  • The Chaim Sheba Medical Center /ID# 261699 โ€” Ramat Gan, Tel Aviv
  • Tel Aviv Sourasky Medical Center /ID# 261525 โ€” Tel Aviv, Tel Aviv
  • Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital /ID# 265286 โ€” Nagoya, Aichi-ken
  • Kindai University Hospital /ID# 266016 โ€” Sakai-shi, Osaka

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Multiple Myeloma clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—