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Search / Trial NCT04025515

Molecular Profiling Project

Launched by NATIONAL CANCER CENTRE, SINGAPORE · Jul 18, 2019

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Oncomine Focus Panel Assay Molecular Profiling Targeted Therapies Driver Oncogene Next Generation Sequencing (Ngs) Pd L1 Immunohistochemistry (Ihc, Dako 22 C3) Hotspots Single Nucleotide Variants (Sn Vs) Insertions/ Deletions (Indels) Copy Number Variation (Cn Vs), Gene Fusions Formalin Fixed Paraffin Embedded (Ffpe) Extracted Dna And Rna Ion Pgm™ System Oncomine™ Comprehensive Assay V3

ClinConnect Summary

The Molecular Profiling Project is a clinical trial focused on understanding the different genetic types of non-small cell lung cancer in patients. The researchers aim to analyze tumor samples to identify specific genetic changes that could affect how the cancer behaves and how it can be treated. This study is currently recruiting participants aged 21 and older who have enough tumor tissue available for testing and can meet certain health criteria, such as having a good level of organ function.

If you or someone you know is interested in participating, they should have a life expectancy of at least 12 weeks and be willing to undergo routine blood tests to ensure they are eligible. Participants can expect to provide a tumor sample and to be a part of research that may help improve future treatments for lung cancer. Remember, if someone does not meet all the standard criteria, there may still be a chance to discuss enrollment with the study team on a case-by-case basis.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • The availability of sufficient archival tumor tissue specimen (15 slides of 4 microns per section)
  • Age ≥ 21 years
  • WHO performance status ≤ 2
  • Life expectancy of ≥ 12 weeks
  • * Patients should have adequate organ function for potential consideration into clinical trials (routine blood tests are valid within 14 days before enrollment):
  • Adequate bone marrow function as shown by: ANC ≥ 1.0 x 10\^9/L, Platelets ≥ 75 x 10\^9/L, Hb ≥ 7.5 g/dL
  • Alanine aminotransferase (ALT) and aspirate aminotransferase (AST) normal range (or ≤3.0 x ULN if liver metastases are present)
  • Willing to provide signed informed consent
  • Patients whom do not fulfill the above criteria may be discussed on a case-by-case basis with the study team, for potential enrolment
  • Exclusion Criteria:
  • - No more than 3 lines of cytotoxic chemotherapy at the time of enrolment

About National Cancer Centre, Singapore

The National Cancer Centre Singapore (NCCS) is a leading institution dedicated to cancer treatment, research, and education in Asia. As a premier clinical trial sponsor, NCCS focuses on advancing oncology through innovative therapies and comprehensive clinical studies. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to improving patient outcomes and contributing to global cancer research initiatives. NCCS actively collaborates with various stakeholders, including academic institutions and pharmaceutical companies, to foster groundbreaking discoveries and enhance the understanding of cancer management and treatment.

Locations

Singapore, , Singapore

Bangkok, , Thailand

Hong Kong, , Hong Kong

Petaling Jaya, , Malaysia

Hong Kong, , Hong Kong

Kuala Lumpur, , Malaysia

Brunei, , Brunei Darussalam

New Delhi, , India

Kuala Lumpur, , Malaysia

Penang, , Malaysia

Patients applied

0 patients applied

Trial Officials

Daniel Tan, BSc, MBBS, MRCP

Principal Investigator

National Cancer Centre, Singapore

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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