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NCT06976476RecruitingPhase 2

Study of IgPro20 to Prevent Infection in People With Multiple Myeloma and Hypogammaglobulinemia

Prospective Randomized Phase II Study Evaluating Efficacy and Safety of IgPro20 as Infection Prophylaxis in Patients With Multiple Myeloma and Hypogammaglobulinemia Receiving Therapy With a Bispecific Monoclonal Antibody (BsAbs)

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

The main purpose of this study is to see if IgPro20 can prevent infection in people with multiple myeloma (MM) who have hypogammaglobulinemia from receiving bispecific monoclonal antibodies (BsAbs).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
First submitted
8 May 2025
Start date
8 May 2025
Primary completion date
8 May 2029
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT06976476

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 100
  • From 8 May 2025 to the primary completion date, 8 May 2029
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • HSCT within 3 months before enrollment
  • Planned CAR-T therapy in the next 6 months
  • On current or previous IVIG (in the last 3 months)

Other illness

  • \>1 major (deep-seated) infection within the preceding 3 months
  • HIV infection, Active HCV, or Active HBV infection
  • History of cancer other than MM in the last 3 years requiring active chemotherapy or radiation
  • Known reaction/allergy to IgG products
  • Intracranial hemorrhage or embolic CVA in the last 6 months
  • Known history of Hyperprolinemia

Lab values

  • Neutrophils \< 500 x 10\^3 per mL, Platelets \< 30 x 10\^9 per mL
  • Creatinine Cl \<30 ml/min

Other

  • Pregnancy
  • Hyperproteinemia
  • Protein-losing enteropathy
  • Documented progression on BsAb

Who the study is looking for

  • Diagnosis of RRMM receiving a commercially available bispecific antibody
  • Received at least 1 but no more than 4 cycles of BsAb
  • Males or females greater than or equal to 18 years old at the time of consent
  • ECOG ≤ 3
  • Life expectancy \> 12 months

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University (Data Collection Only)
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Memorial Sloan Kettering Suffolk-Commack (All protocol activity)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (All Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (All Protocol Activities)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
Mount Sinai Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesNot yet recruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Memorial Sloan Kettering Nassau (All Protocol Activities)
Coordinator of this site? Confirm its status
UniondaleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.