RecruitingPhase 1NCT06507306

A Study to Investigate the Safety and Efficacy of KQB198 as Monotherapy and in Combination in Participants With Advanced Solid Malignancies

A Phase 1/1b, Open-label, Multicenter, Dose Escalation and Dose Expansion Study Evaluating the Safety, Tolerability, Pharmacokinetics and Efficacy of KQB198 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Malignancies


Sponsor

Kumquat Biosciences Inc.

Enrollment

100 participants

Start Date

Jun 3, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn if KQB198 works to treat advanced solid tumor cancer in adults. It will also learn about the safety of KQB198. The main questions it aims to answer are: * What is the safe dose of KQB198 by itself or in combination with other anti-cancer drugs? * Does KQB198 alone or in combination with other anti-cancer drugs decrease the size of the tumor? * What happens to KQB198 in the body? Participants will: * Take KQB198 daily, alone or in combination with another anti-cancer drug * Visit the clinic about 8 times in the first 8 weeks, and then once every 4 weeks after that


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • PART 1 - Histologically confirmed diagnosis of a solid tumor malignancy with any of the following oncogenic mutations: EGFR, RAS, PTPN11, or SOS1 mutations, or inactivating mutations of NF1.
  • PART 1 - (Osimertinib and Amivantamab arms) and Part 2 Cohort A and Cohort B: Histologically confirmed diagnosis of NSCLC with activating EGFR mutation and progression on osimertinib
  • Part 3 - Cohort A: Histologically confirmed diagnosis of NSCLC with exon 20 insertion EGFR mutation
  • Unresectable or metastatic disease
  • No available treatment with curative intent
  • Adequate organ function
  • Measurable disease per RECIST 1.1.

Exclusion Criteria4

  • Prior therapy with a similar mechanism of action to KQB198
  • History of intestinal disease, inflammatory bowel disease, major gastric surgery, or other gastrointestinal conditions likely to alter absorption of study treatment or result in inability to swallow
  • History of interstitial lung disease
  • Cardiac abnormalities

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Interventions

DRUGKQB198

Oral KQB198

DRUGOsimertinib

Oral Osimertinib

DRUGAmivantamab

Subcutaneous administration


Locations(35)

Sarah Cannon Research Institute at HealthONE

Denver, Colorado, United States

Sarah Cannon Research Institute at Florida Cancer Specialists - Lake Nona -

Orlando, Florida, United States

Florida Cancer Specialists - Sarasota

Sarasota, Florida, United States

Henry Ford Health System

Detroit, Michigan, United States

David H. Koch Center for Cancer Center at Memorial Sloan Kettering Cancer Center

Long Island City, New York, United States

The Lindner Center for Research and Education at The Christ Hospital

Cincinnati, Ohio, United States

Sarah Cannon and HCA Research Institute

Nashville, Tennessee, United States

MD Anderson Cancer Center

Houston, Texas, United States

New Experimental Therapeutics of San Antonio - NEXT Oncology

San Antonio, Texas, United States

New Experimental Therapeutics of Virginia - NEXT Oncology

Fairfax, Virginia, United States

Institut Paoli-Calmettes

Marseille, Bouches-du-Rhône, France

Institut de Cancerologie de l'Ouest - site St-Herblain

Saint-Herblain, Loire-Atlantique, France

CHU Bordeaux - Hopital Saint-Andre

Bordeaux, Nouvelle-Aquitane, France

IUCT-Oncopole

Toulouse, Occitaine, France

CHU de Nantes - Hopital Nord Laennec

Nantes, Pays de la Loire Region, France

Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore

Rome, Lazio, Italy

Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"

Naples, Italy

National Cancer Center

Goyang-si, Gyeonggi-do, South Korea

Chonnam National University Hwasun Hospital

Hwasun, Jeollanam-do, South Korea

Severance Hospital, Yonsei University Health System

Seoul, South Korea

Seoul St. Mary's Hospital, The Catholic University of Korea

Seoul, South Korea

Hospital Universitari Quiron Dexeus Barcelona

Barcelona, Catalonia, Spain

Hospital Universitario Vall d'Hebron

Barcelona, Catalonia, Spain

New Experimental Therapeutics (NEXT) Oncology Barcelona

Barcelona, Spain

South Texas Accelerated Research Therapeutics (START) Barcelona- HM Nou Delfos

Barcelona, Spain

Hospital Universitario Ramon y Cajal

Madrid, Spain

South Texas Accelerated Research Therapeutics (START) Madrid - CIOCC

Madrid, Spain

New Experimental Therapeutics (NEXT) Oncology Madrid - Hospital Quironsalud Madrid

Madrid, Spain

South Texas Accelerated Research Therapeutics (START) Madrid - Hospital Fundacion Jimenez Diaz

Madrid, Spain

Hospital Quirónsalud Málaga

Málaga, Spain

Clinica Universidad de Navarra - Pamplona

Pamplona, Spain

Chi-Mei Hospital - Liouying Branch

Liuying, Tainan City, Taiwan

National Taiwan University Hospital

Taipei, Taipei City, Taiwan

Taichung Veterans General Hospital

Taichung, Taiwan

Taipei Veterans General Hospital

Taipei, Taiwan

View Full Details on ClinicalTrials.gov

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NCT06507306


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