Amgen, 20230153, Ph 2, randomized, open-label, NSCLC, AMG193

What is the Purpose of this Study?

Primary Objective: To characterize safety and efficacy of 2 dose levels of AMG 193 by investigator.


Eligibility

  • * Histologically or cytologically confirmed metastatic or unresectable locally advanced MTAP-deleted (Homozygous deletion of MTAP in the tumor tissue) non-small cell lung cancer
  • * Participants will have received and progressed or experienced disease recurrence on or after receiving at least 1 prior systemic therapy for locally advanced and unresectable or metastatic disease.
  • * Either an archival tissue sample or an archival block must be available.
  • * Life expectancy of greater than 3 months, in the opinion of the investigator.
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Where can I participate?

CS Cancer at Cedars-Sinai Medical Center : Garrett Crook

More about this Clinical Trial

What is the full name of this clinical trial?

20230153: A Phase 2 Study Evaluating the Efficacy, Safety, Tolerability, and Pharmacokinetics of AMG 193 in Subjects with Methylthioadenosine Phosphorylase -deleted Previously Treated Advanced Non-Small Cell Lung Cancer

Study Details
Disease Type/Condition

Lung

Principal Investigator

Sankar, Kamya

Co-Investigators

Karen Reckamp, Navid Hafez

Age Group

Adult

Phase

II

IRB Number

STUDY00003730

ClinicalTrials.gov ID

NCT06593522

Key Eligibility
ClinicalTrials.gov

How do I learn more about this study?
Name

Garrett Crook

Email
Garrett.Crook@cshs.org
Study Detail
Disease Type/Condition

Lung

Principal Investigator

Sankar, Kamya

Age Group

Adult

Phase

II

IRB Number

20230153

ClinicalTrials.gov ID

NCT06593522

Key Eligibility
ClinicalTrials.gov

Contact
Name

Garrett Crook

Email
Garrett.Crook@cshs.org