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Leállítva1. fázis

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

A legfontosabb adatok

Ki végzi
NiKang Therapeutics, Inc.
Hol
Augusta, Austin, Canton, Celebration, Denver, Louisville, San Francisco és West Valley City (Egyesült Államok)Mind a 8 helyszín megnézése
Azonosító
Állapot
Leállítva
Fázis
1. fázis
Résztvevők
23 fő vett részt
Kezdés
2024. febr. 23.
Befejezés
2025. ápr. 16.
A vizsgálat típusa
Beavatkozással járó, 2 csoport
A vizsgált kezelések
  • NKT3447
A regiszteradat frissítve
2025. szeptember 25.
Miért állt le
This study was terminated as a result of Sponsor portfolio reprioritization.

Ki vehet részt

Életkor
18 év felett
Nem
Nők és férfiak
Egészséges önkéntesek
Nem vehetnek részt

A regiszter feltételei, szó szerint

Mind a 21 feltétel megnézéseKevesebb

Ki vehet részt

  • 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):
  • 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

Ki nem vehet részt

  • Locally advanced solid tumor that is a candidate for curative treatment through radical surgery and/or radiotherapy, or chemotherapy
  • Failed to recover from effects of prior anticancer treatment therapy to baseline or Grade ≤ 1 severity (per CTCAE)
  • Prior CDK2 inhibitor
  • Major surgery within 2 months or minor surgery within 10 days before the first dose of NKT3447
  • History of another malignancy with exceptions
  • 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
  • Visceral crisis with life-threatening complications, lymphangitic spread, CNS metastasis and/or carcinomatous meningitis

Helyszínek itt: Egyesült Államok

  • Augusta University, Georgia Cancer CenterAugusta, Egyesült Államok
  • Texas Oncology-Austin Midtown NEXT OncologyAustin, Egyesült Államok
  • The Gabrail Pharmacology Phase 1 Research CenterCanton, Egyesült Államok
  • AdventHealth Cancer InstituteCelebration, Egyesült Államok
  • Sarah Cannon Research Institute at HealthONEDenver, Egyesült Államok
  • Norton Cancer Institute - BroadwayLouisville, Egyesült Államok
  • University of California San Francisco (UCSF) - Helen Diller Family Comprehensive Cancer CenterSan Francisco, Egyesült Államok
  • START Mountain RegionWest Valley City, Egyesült Államok

A vizsgálatról

Mit akar kideríteni a vizsgálat

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).

A vizsgálat 2 csoportja

  • Dose EscalationA vizsgált kezelés

    Dose escalation will assess the safety, efficacy, and PK/PD data of oral dosing NKT3447 at increasing dosage levels to determine the MTD and/or preliminary RDEs.

    Kezelés: NKT3447

  • Dose ExpansionA vizsgált kezelés

    Dose expansion will include 2 RDEs selected to determine the preliminary antitumor activity and the RP2D.

    Kezelés: NKT3447

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
A Phase 1, First-in-Human, Open-Label Study to Evaluate the Safety, Tolerability, PK, and Preliminary Anti-tumor Activity of the Novel Orally Available CDK2 Inhibitor NKT3447 in Adults With Advanced/Metastatic Solid Tumors
A regiszteradat frissítve
2025. szeptember 25.