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DRUG:

IK-175

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Other names: IK-175, KYN-175
Company:
Ikena Oncology
Drug class:
AHR antagonist
Related drugs:
2ms
Oral AHR Antagonist in Combination With Nivolumab in Patients With PD-1 Resistant Metastatic or Recurrent Head and Neck Cancer (clinicaltrials.gov)
P1, N=0, Withdrawn, Ikena Oncology | Phase classification: P1b --> P1 | N=54 --> 0 | Trial completion date: Jul 2025 --> Apr 2023 | Not yet recruiting --> Withdrawn | Trial primary completion date: Jul 2024 --> Apr 2023
Phase classification • Enrollment change • Trial completion date • Trial withdrawal • Trial primary completion date • Combination therapy • Metastases
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PD-L1 (Programmed death ligand 1)
|
PD-L1 expression
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Opdivo (nivolumab) • IK-175
2ms
A Phase 1a/b Study of IK-175 as a Single Agent and in Combination With Nivolumab in Patients With Locally Advanced or Metastatic Solid Tumors and Urothelial Carcinoma (clinicaltrials.gov)
P1, N=78, Completed, Ikena Oncology | Recruiting --> Completed | Trial completion date: Sep 2022 --> Jul 2023 | Trial primary completion date: Sep 2022 --> Jul 2023
Trial completion • Trial completion date • Trial primary completion date • Combination therapy • Checkpoint inhibition • Metastases
|
Opdivo (nivolumab) • IK-175
almost2years
Discovery and characterization of a novel aryl hydrocarbon receptor inhibitor, IK-175, and its inhibitory activity on tumor immune suppression. (PubMed, Mol Cancer Ther)
These studies provide rationale for targeting AHR in cancer patients. IK-175 is being evaluated in a Phase 1 clinical trial in patients with advanced solid tumors.
Journal • PD(L)-1 Biomarker • IO biomarker
|
IL17A (Interleukin 17A) • IL22 (Interleukin 22) • CYP1A1 (Cytochrome P450 Family 1 Subfamily A Member 1)
|
IK-175
almost2years
New P1 trial • Combination therapy
|
PD-L1 (Programmed death ligand 1)
|
PD-L1 expression
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Opdivo (nivolumab) • IK-175
over2years
Analytical validation of a novel immunohistochemistry assay to determine nuclear AHR expression in human bladder cancer (SITC 2021)
IK-175 is being evaluated in an ongoing phase 1 clinical study as a single agent and in combination with nivolumab for bladder cancer patients (NCT04200963). Conclusions A novel and robust nuclear AHR IHC assay for bladder cancer was developed and analytically validated in a CLIA certified lab and showed ≥95% accuracy, specificity, sensitivity, and precision, enabling its implementation in an IK-175 Ph1b clinical study (NCT04200963) for prospective patient enrichment. Trial Registration NCT04200963
PD(L)-1 Biomarker • IO biomarker
|
AHR (Aryl hydrocarbon receptor)
|
AHR expression
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Opdivo (nivolumab) • IK-175