A Study With NKT3447 for Adults With Advanced/Metastatic Solid Tumors

Stopped early · Phase 1

Conditions studied: Solid Tumor, Solid Tumor, Adult, Advanced Solid Tumor, Metastatic Tumor, Ovarian Cancer, Ovarian Neoplasms, Ovarian Carcinoma, Metastatic Ovarian Carcinoma, Endometrial Cancer, Endometrial Neoplasms, Endometrial Diseases, Metastatic Endometrial Cancer, Metastatic Endometrial Carcinoma, Advanced Endometrial Carcinoma, Advanced Ovarian Carcinoma, Gastric Cancer, Advanced Gastric Carcinoma, Metastatic Gastric Cancer, Metastatic Gastric Carcinoma, Small-cell Lung Cancer, Small Cell Lung Carcinoma, Triple Negative Breast Cancer, Triple Negative Breast Neoplasms, Platinum-resistant Ovarian Cancer, Platinum-refractory Ovarian Carcinoma, CCNE1 Amplification, Hormone Receptor Negative Breast Carcinoma, Human Epidermal Growth Factor 2 Negative Carcinoma of Breast, Progesterone-receptor-positive Breast Cancer

In brief

The goal of the Dose Escalation phase of the study is to evaluate the safety, tolerability, and pharmacokinetics (PK) to determine the maximum tolerated dose (MTD) and/or preliminary recommended dose for expansion (RDE) of NKT3447 in adults with advanced or metastatic solid tumors. The goal of the Expansion phase of the study is to evaluate the safety, tolerability, pharmacokinetics (PK), and the preliminary antitumor activity of NKT3447 in adult subjects with cyclin E1 (CCNE1) amplified ovarian cancer at the RDEs selected in Dose Escalation and to determine the preliminary recommended phase 2 dose (RP2D).

Key facts

Study ID

NCT06264921

Run by

NiKang Therapeutics, Inc.

People needed

23

Starts

2024-02-23

Expected to finish

2025-04-16

Last updated by the study team

2025-09-25

Who can join

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

You may qualify if…

• Must have confirmed unresectable advanced/metastatic solid tumors (as outlined below) with disease progression on prior standard treatment, intolerance to or ineligibility for standard treatment, or no available standard treatment likely to improve the disease outcome in the judgment of the Investigator.
• Measurable disease per the RECIST v1.1
• An Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
• Able to swallow oral medications.
• Dose Escalation(Part 1):
• Ovarian cancer
• Endometrial cancer
• Gastric cancer or gastroesophageal junction cancer
• Small cell lung cancer (SCLC)
• Triple-negative breast cancer (human epidermal growth factor receptor 2 [HER2], estrogen receptor [ER], progesterone receptor negative)
• ER/progesterone-receptor positive, HER2 negative breast cancer (must have progressed following treatment with a CDK4/6 inhibitor, and not suitable for endocrine therapy)
• Other solid tumors with CCNE1 amplification as determined by NGS by local liquid or tissue biopsy.
• Dose Expansion (Part 2):
• a. Platinum resistant or refractory ovarian cancer (defined as recurrence ≤6 months after completing platinum-based regimen) with progression on at least 1 platinum containing therapy with CCNE1 amplification as determined by NGS by local liquid or tissue biopsy.
• Measurable disease per the RECIST v1.1
• An Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
• Able to swallow oral medications.

You may not qualify if…

• Locally advanced solid tumor that is a candidate for curative treatment through radical surgery and/or radiotherapy, or chemotherapy.
• History of another malignancy with exceptions
• Visceral crisis with life-threatening complications, lymphangitic spread, CNS metastasis and/or carcinomatous meningitis
• Failed to recover from effects of prior anticancer treatment therapy to baseline or Grade ≤ 1 severity (per CTCAE)
• Clinically active interstitial lung disease
• History of uveitis, retinopathy or other clinically significant retinal disease
• Has known human immunodeficiency virus (HIV), active hepatitis B or C infection
• Prior CDK2 inhibitor
• Major surgery within 2 months or minor surgery within 10 days before the first dose of NKT3447

Where it is running

• University of California San Francisco (UCSF) - Helen Diller Family Comprehensive Cancer Center — San Francisco, California, United States
• Sarah Cannon Research Institute at HealthONE — Denver, Colorado, United States
• AdventHealth Cancer Institute — Celebration, Florida, United States
• Augusta University Georgia Cancer Center — Augusta, Georgia, United States
• Norton Cancer Institute - Broadway — Louisville, Kentucky, United States
• The Gabrail Pharmacology Phase 1 Research Center — Canton, Ohio, United States
• Texas Oncology-Austin Midtown NEXT Oncology — Austin, Texas, United States
• START Mountain Region — West Valley City, Utah, United States

Full record on ClinicalTrials.gov

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