IDP-023
DrugNK cell therapy
NCT Number: NCT06119685
This is an open label, Phase 1/2, first-in-human, multiple ascending dose, and dose-expansion study of IDP-023 administered as a single agent and in combination with or without interleukin-2 (IL-2), and with or without isatuximab, daratumumab or rituximab to evaluate the safety, tolerability and preliminary antitumor activity in patients with advanced hematologic cancers.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Valkyrie Clinical Trials, Los Angeles, California, United States
IDP-023 is an off-the-shelf, allogeneic cell product made of "natural killer" cells, also called NK cells. White blood cells are part of the immune system and NK cells are a type of white blood cell that are known to kill cancer cells.
This is an open label, Phase 1/2, first-in-human, multiple ascending dose, and dose-expansion study of IDP-023 administered as a single agent and in combination with or without interleukin-2 (IL-2), and with or without isatuximab, daratumumab or rituximab to evaluate the safety, tolerability, and preliminary antitumor activity in patients with relapsed and/or refractory advanced multiple myeloma (MM) or non-Hodgkin's lymphoma (NHL), respectively.
The study is divided into a phase 1 dose escalation phase and a phase 2 expansion phase.
Phase 1 (Escalation Phase): The primary objectives of Phase 1 are to define the safety of different IDP-023 containing regimens and to define the recommended regimen and Phase 2 doses (RP2D) of IDP-023.
Phase 2 (Expansion Phase): The objective of the Phase 2 expansion cohort is to evaluate the safety and efficacy of IDP-023 in advanced MM in combination with isatuximab or daratumumab and advanced NHL in combination with rituximab.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
NK cell therapy
Anti-CD20 antibody therapy
Other names: Rituxan
Anti-CD38 antibody therapy
Other names: Darzalex
Immune cytokine
Other names: Proleukin
Lymphodepleting chemotherapy
Lymphodepleting chemotherapy
Chemoprotectant
Anti-CD38 antibody therapy
Other names: Sarclisa
Time frame: 1 year
Escalation Period
Time frame: up to 21 days
Escalation Period
Time frame: up to 21 days
Escalation Period
Time frame: up to 35 days
Escalation Period
Time frame: up to 35 days
Escalation Period
Time frame: 1 year
Escalation Period
Time frame: 2 years
Expansion period
Time frame: 2 years
Expansion period
Time frame: 2 years
Escalation and expansion periods
Time frame: 2 years
Escalation and expansion periods
Time frame: 1 year
Escalation period
Time frame: 1 year
Escalation period
Time frame: 2 years
Expansion period
Contact information is provided by the study sponsor or research team.
Indapta Therapeutics, INC.
Industry
Phase 1/2 Study of IDP-023 as a Single Agent and in Combination With Antibody Therapies in Patients With Advanced Hematologic Cancers
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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