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IPH2102 at/kg

Phase 2

Acute Myeloid Leukemia | Small molecule | Oncology |Innate Pharma S.A.|Last Updated: Feb 8, 2019

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLEDDMC
Total Trials1
Total Enrollment152

FDA Designations

No designations recorded

Clinical trial landscape

IPH2102 at/kg · 1 trial · 1 indication

Phase 2 1
NCT01687387Efficacy Study of Anti-KIR Monoclonal Antibody as Maintenance Treatment in Acute Myeloid Leukemia (EFFIKIR)Acute Myeloid Leukemia
COMPLETED152 Analytics
PHASE2COMPLETED
Efficacy Study of Anti-KIR Monoclonal Antibody as Maintenance Treatment in Acute Myeloid Leukemia (EFFIKIR)
Acute Myeloid LeukemiaUnlock trial analytics

Study Endpoints

Primary Endpoints

Leukemia-Free Survival
from date of randomization until the date of first documented relapse, assessed up to 48 months

Secondary Endpoints

Number of Participants With Adverse Events
from the time of patient signing the consent form until 28 days after the last administration, or until the patient's last study visit, up to 24 months
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
IPH2102 at 1 mg/kgEXPERIMENTALlirilumab (IPH2102/BMS986015) at 1 mg/kg
IPH2102 at 0.1 mg/kgEXPERIMENTALlirilumab (IPH2102/BMS986015) at 0.1 mg/kg
Placebo (Normal saline solution)PLACEBO_COMPARATORNormal saline solution

Interventions

NameTypeDescription
IPH2102 at 0.1 mg/kgDRUGevery 3 months
IPH2102 at 1 mg/kgDRUGevery 4 weeks
Placebo (normal saline solution)DRUGevery 4 weeks
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Eligibility Criteria

Age Range60 Years to 80 Years
SexALL
Healthy VolunteersNo
Study Sites43

Inclusion Criteria: 1. Primary or secondary Acute Myeloid Leukemia (AML, defined according to WHO 2008 criteria), in first CR/CRi (according to the revised recommendations of the International Working Group for Diagnosis, Standardization of Response Criteria, Treatment Outcomes, and Reporting Stand...

Countries:France
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Frequently asked questions about IPH2102 at/kg

What is IPH2102 at/kg used for in Acute Myeloid Leukemia?

IPH2102 at/kg is an investigational small molecule being studied as a maintenance treatment for Acute Myeloid Leukemia (AML). It is being evaluated in a Phase 2 clinical trial to assess its efficacy in patients aged 60 years and older. The drug is not yet approved and remains in clinical development.

What does IPH2102 at/kg target?

IPH2102 at/kg is a monoclonal antibody that targets KIR (killer cell immunoglobulin-like receptors) on natural killer cells. By blocking these receptors, it aims to enhance the immune system's ability to attack cancer cells. This mechanism is being investigated in the context of Acute Myeloid Leukemia maintenance therapy.

Who makes IPH2102 at/kg?

IPH2102 at/kg is being developed by Innate Pharma S.A., a biopharmaceutical company. The company is conducting clinical trials to evaluate the drug's safety and efficacy in patients with Acute Myeloid Leukemia. Innate Pharma is listed on the stock exchange under the ticker IPHA.

What phase is IPH2102 at/kg in?

IPH2102 at/kg is currently in Phase 2 clinical development. It is being studied as a maintenance treatment for Acute Myeloid Leukemia. The drug is investigational and has not been approved by regulatory authorities. A Phase 2 trial has been completed to evaluate its efficacy.

What clinical trials is IPH2102 at/kg in?

IPH2102 at/kg has one completed Phase 2 clinical trial with the identifier NCT01687387. The trial, titled 'Efficacy Study of Anti-KIR Monoclonal Antibody as Maintenance Treatment in Acute Myeloid Leukemia (EFFIKIR)', enrolled 152 participants in France. The study was randomized, double-blind, and placebo-controlled, involving patients aged 60 years and older.

Is IPH2102 at/kg the same as anti-KIR monoclonal antibody?

IPH2102 at/kg is an anti-KIR monoclonal antibody, as indicated by the clinical trial title. It is designed to target KIR receptors. The drug is being investigated for its potential role in maintenance treatment of Acute Myeloid Leukemia, though it remains in clinical development and is not yet approved.