A Clinical Study of KK2260 in Patients With Advanced or Metastatic Solid Tumors

Recruiting now · Phase 1

Conditions studied: Advanced or Metastatic Solid Tumors

In brief

This is the first in human study of KK2260. In Part 1a, the maximum tolerated dose (MTD) will be determined while evaluating the safety and tolerability of KK2260 in patients with advanced or metastatic solid tumors (any cancer type). In Part 1b and Part 2, at least two dosing regimens and two dosing regimens by cancer type, respectively, will be selected, and the safety, tolerability, and efficacy of each regimen will be evaluated.

Key facts

Study ID: NCT06248411
Run by: Kyowa Kirin Co., Ltd.
People needed: 189
Starts: 2023-11-01
Expected to finish: 2030-04-30
Last updated by the study team: 2026-05-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

<Common Inclusion Criteria for Part 1a, Part 1b, and Part 2
Patients who have given informed written consent.
Male or female subjects ≥18 years of age, at time of signing informed consent.
Subjects who are refractory to standard treatment, intolerant of standard treatment, for whom standard treatment does not exist, or who have refused standard treatment.
Patients with measurable disease according to RECIST version 1.1
Patients who have had the certaion periods between the date of completion of prior therapy and the date of enrollment
Subjects who agree to have a tumor biopsy as part of the baseline examination. Patients who have difficulty in performing a tumour biopsy and have agreed to submit a previously collected stored specimen.
Patients with an ECOG PS of 0 or 1 at baseline.
Patients with haematopoietic, hepatic, renal, cardiac and respiratory functions that meet certain criteria in a baseline test.
<Additional Inclusion Criteria for Part 1a
Patients with pathologically diagnosed advanced or metastatic solid tumors.
<Additional Inclusion Criteria for Part 1b
Patients with pathologically diagnosed with advanced or metastatic esophageal cancer, or advanced or metastatic head and neck cancer whose primary site of origin is the oral cavity, oropharynx, hypopharynx, larynx, nasal cavity, or paranasal sinuses.
Patients with pathologically diagnosed squamous cell carcinoma.
Patients who agree to undergo tumor biopsy after administration.
<Additional Inclusion Criteria for Part 2a
Patients with pathologically diagnosed with advanced or metastatic esophageal cancer.
Patients with pathologically diagnosed squamous cell carcinoma.
Patients who agree to undergo tumor biopsy after administration.
<Additional Inclusion Criteria for Part 2b
Patients with advanced or metastatic head and neck cancer whose primary site of origin is the oral cavity, oropharynx, hypopharynx, larynx, nasal cavity, or paranasal sinuses.
Patients with pathologically diagnosed squamous cell carcinoma.
Patients who agree to undergo tumor biopsy after administration.

You may not qualify if…

<Common Exclusion Criteria to Part 1 and Part 2>
Patients with central or brain pia mater metastases that are untreated and symptomatic or that require treatment.
Patients with concurrent multiple or synchronous cancers, or with iatrogenic multiple or synchronous cancers with a disease-free interval of 5 years or less.
Patients receiving continuous systemic administration of steroids or other immunosuppressive drugs.
Patients who have had a Grade 3 or higher allergic reaction to an antibody agent or an additive of the study drug.
Patients who have not recovered to Grade 1 or below from adverse events caused by previously administered anticancer therapy.
Patients with active interstitial lung disease or a history of active interstitial lung disease.
Patients with infectious diseases requiring systemic treatment.
Patients with a fever of 38.0°C or higher at the time of registration.
Patients who test positive for Hepatitis B virus antigen or antibody, Hepatitis C virus antibody, or HIV antibody in a baseline test.

Where it is running

Aichi Cancer Center Hospital — Nagoya, Aichi-ken, Japan (enrolling)
National Cancer Center Hospital East — Kashiwa, Chiba, Japan (enrolling)
Shikoku Cancer Center — Matsuyama, Ehime, Japan (enrolling)
Hiroshima University Hospital — Hiroshima, Hiroshima, Japan (enrolling)
Kobe University Hospital — Kobe, Hyōgo, Japan (enrolling)
Kanagawa Cancer Center — Yokohama, Kanagawa, Japan (enrolling)
Kumamoto University Hospital — Kumamoto, Kumamoto, Japan (enrolling)
Tohoku University Hospital — Sendai, Miyagi, Japan (enrolling)
Saitama Cancer Center — Shinden, Saitama, Japan (enrolling)
Shizuoka Cancer Center — Nagaizumi-cho, Shizuoka, Japan (enrolling)
National Cancer Center Hospital — Chuo-ku, Tokyo, Japan (enrolling)
The Cancer Institute Hospital of JFCR — Koto-ku, Tokyo, Japan (enrolling)
Kyushu Cancer Center — Fukuoka, Japan (enrolling)
Osaka International Cancer Institute — Osaka, Japan (enrolling)

Full record on ClinicalTrials.gov

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