About this trial

A total of at least 1,000 participants with suspicion of cancer including at least 107 subjects who will be diagnosed with OSCC or OPSCC will be enrolled from either primary or secondary care centers in the U.S. Clinicians will use Viome collection kits to collect saliva samples from eligible patients.

Eligibility criteria

Qualifiers

Signed and dated informed consent prior to any study-specific procedures are performed

Willing and able to follow the study instructions, as described in the recruitment letter

Adults (18 years old or older)

Suspicion of OSCC or OPSCC on clinical presentation by a clinician

Disqualifiers

Pregnancy

Use of fertility enhancing medications

Trial design

Treatments tested in this trial

  • Oral/Throat cancer test

Treatment groups

1,000 Participants
are divided into 3 treatment groups

Locations

2
Missouri School of Dentistry & Oral Health63104, St LouisMissouri, United States
UTHSC38163, MemphisTennessee, United States

Sponsors and collaborators

Viome

Lead sponsor