Clinical trial · Interventional
Study on the Anti-tumor Activity, Safety and Pharmacology of IPH2101 in Patients With Smoldering Multiple Myeloma
Multicenter Phase II Study on the Anti-tumor Activity, Safety and Pharmacology of Two Dose Regimens of IPH2101, a Fully Human Monoclonal Anti KIR Antibody, in Patients With Smoldering Multiple Myeloma (KIRMONO)
NCT01222286CI-TRIAL-00111584KIRMONOcompletedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the anti-tumor activity, safety and pharmacology of two dose regimens (0.2 and 2 mg/kg)of IPH2101 in patients with Smoldering Multiple Myeloma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Smoldering Multiple Myeloma | Smoldering Multiple Myeloma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| IPH2101 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- IPH2101 0.2 mg/kg
- description
- 0.2 mg/Kg every 4 weeks by intravenous route over 1 hour, for 6 or up to 12 cycles
- interventionNames
- Drug: IPH2101
- type
- EXPERIMENTAL
- label
- IPH2101 2 mg/kg
- description
- 2 mg/Kg every 4 weeks by intravenous route over 1 hour, for 6 or up to 12 cycles
- interventionNames
- Drug: IPH2101
Primary outcomes (1)
- measure
- Rate of Patients Achieving an Objective Response
- timeFrame
- from start to end of study (14 months)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. SMM of any risk level according to a definition derived of the International Myeloma Working Group definition ( Br J Haematol 2003; 121: 749) : Serum M protein ≥ 3 g/dl , AND/OR Bone Marrow plasma cells ≥ 10 % with no evidence of end-organ damage (CRAB) * (C)Absence of hypercalcemia : Ca \< 10.5 mg/dl * (R)Absence of renal failure : creatinine \< 2mg/dl (177 μmol/l) or calculated creatinine clearance(according to MDRD) \> 50 ml/min * (A)Absence of anemia : Hb \> 11 g/dl * (B)Absence of lytic bone lesion on standard skeletal survey (MRI could be used if clinically indicated) 2. Measurable disease defined as a disease with a serum M protein ≥ 1 g/dl 3. No evidence of fatigue, recurrent infections or any clinical suspicion of MM 4. Diagnosis of SMM confirmed on two consecutive assessments (ie fluctuation under 25% of serum protein level) performed with at least a 4 week interval. 5. Age \> 18 years or \< 75 years 6. ECOG performance status of 0 or 1 7. Male or female patient who accepts and is able to use recognised effective contraception (oral contraceptives, IUCD, barrier method of contraception in conjunction with spermicidal jelly) throughout the study when relevant 8. Informed consent signed by the patient Exclusion Criteria: 1. Previous treatment having a proven or potential impact on myelomatous cells proliferation or survival (including IMiDs or proteasome inhibitors, conventional chemotherapies within the last 5 years, steroids within the last month prior to enrolment). Previous bisphosphonates started less than 3 months prior to enrolment. 2. Use of any investigational agent within the last 3 months 3. Clinical laboratory values at screening * Platelet \< 75 x 10\^9 /l * ANC \< 1.5 x 10\^9 /l * Bilirubin levels \>1.5 ULN ; ALT and AST \> 3 ULN (grade 1 NCI) 4. Primary or associated amyloidosis 5. Abnormal cardiac status with any of the following 1. NYHA stage III or IV congestive heart failure 2. myocardial infarction within the previous 6 months 3. symptomatic cardiac arrhythmia requiring treatment or persisting despite appropriate treatment 6. Current active infectious disease or positive serology for HIV, HCV or positive Hbs Antigen 7. History of or current auto-immune disease 8. History of other active malignancy within the past five years (apart from basal cell carcinoma of the skin, or in situ cervix carcinoma). 9. Serious concurrent uncontrolled medical disorder 10. History of allograft or solid organ transplantation 11. Pregnant or lactating women 12. Any condition potentially hampering compliance with the study protocol and follow-up schedule
References
Publications (0)
Data not yet available
No reference posted for this study.