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Invariant Natural Killer T Cell Therapy

Phase 1

B-Cell ALL | Cell therapy | Other |MiNK Therapeutics, Inc.|Trials Updated: Oct 9, 2026

Invariant Natural Killer T Cell Therapy development status

Highest phase Phase 1
Registered trials 1 across 1 sponsor since Oct 2026

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment13

FDA Designations

No designations recorded

Invariant Natural Killer T Cell Therapy clinical trials

Invariant Natural Killer T Cell Therapy · 1 trial · 4 indications

Phase 1 1
NCT07869368BLinatumomab and iNKT in Relapsed B-Cell ALLB-Cell ALL
NOT YET_RECRUITING13 Analytics
PHASE1NOT YET_RECRUITING
BLinatumomab and iNKT in Relapsed B-Cell ALL
B-Cell ALLUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of participants with Grade 3 or higher Treatment Related Adverse Events -CTCAE
Up to 9 months

Number of participants with Grade 3 or higher Treatment Related Adverse Events based on The NCI Common Terminology Criteria for Adverse Events (CTCAE) will be reported. A grading (severity) scale is provided for each AE term. Grade 1 Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated. Grade 2 Moderate; minimal, local or noninvasive intervention indicated; limiting age-appropriate instrumental Activities of Daily Living (ADL). Grade 3 Severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self-care ADL. Grade 4 Life-threatening consequences; urgent intervention indicated. Grade 5 Death related to AE.

Number of participants with Grade 3 or higher Treatment Related Adverse Events - cytokine release syndrome (CRS)
Up to 9 months

CRS will be graded according to the American Society for Transplantation and Cellular Therapy (ASTCT) CRS Consensus Grading. Grade 1 - Mild: Fever ≥38\^ o C, No hypotension, No hypoxia, Grade 2 - Moderate: Fever ≥38\^ o C, Hypotension not requiring vasopressors, Hypoxia requiring low-flow nasal cannula (≤6 L/minute) or blow-by, Grade 3 - Severe: Fever ≥ 38\^ o C, Hypotension requiring a vasopressor with or without vasopressin, Hypoxia requiring high-flow nasal cannula (\>6 L/minute), facemask, nonrebreather mask, or Venturi mask, Grade 4 - Life-threatening: Fever ≥38\^oC, Hypotension requiring multiple vasopressors (excluding vasopressin), Hypoxia requiring positive pressure (e.g. Continuous positive airway pressure, BiPAP, intubation, mechanical ventilation), Grade 5 - Death

Number of participants with Grade 3 or higher Treatment Related Adverse Events - Neurological Toxicity (ICANS)
Up to 9 months

Immune effector cell-associated neurotoxicity syndrome (ICANS) symptoms will be graded according to the criteria outlined in the protocol on a scale from 1 (mild) to 4 (critical). Cytokine release syndrome (CRS) will be graded according to criteria outlined in the protocol on a scale from 1 (mild) to grade 5 (death).

Secondary Endpoints

The effectiveness of the combination therapy
Up to 9 months
Extramedullary disease response
Up to 42 days (after Cycle 1)
Change in residual B-cell acute lymphoblastic leukemia (B-ALL)
Up to 9 months
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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Blinatumomab-resistant/progressive B-ALLEXPERIMENTALPatients with CD19-positive, Philadelphia chromosome-negative B-ALL with disease progression during blinatumomab therapy, including patients who become MRD-positive after achieving prior MRD negativity or who experience frank relapse.

Interventions

NameTypeDescription
Invariant Natural Killer T Cell TherapyBIOLOGICALAgenT-797 is an investigational invariant natural killer T (iNKT) cell therapy administered as a single intravenous infusion in combination with blinatumomab.
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Written informed consent obtained to participate in the study and HIPAA authorization for release of personal health information. * Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee. * Age ≥ 18 years. * ...

Countries:United States
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