ClinicalTrials.gg
Not yet recruitingNCT06953518Updated May 1, 2025

An Open-Label Pilot Study of Qualia Senolytic Supplementation for the Attenuation of Systemic Inflammatory Cytokines

An interventional study of Qualia Senolytic in Inflammation, sponsored by Qualia Life Sciences. Not yet recruiting at 1 site in United States. Open to participants aged 45 Years to 79 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-01.

Sponsored by Qualia Life Sciences · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 5 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
45 Years to 79 Years
Sex
All
01

Study summary

This open-label pilot study includes adults aged 45 to 79 residing in the United States. The study will last 7 days. Participants will provide blood samples via an at-home finger-prick kit at baseline and day 7 and complete electronic surveys on health indicators at baseline, and days 3 and 7. All procedures are conducted remotely, with no in-person visits, to collect real-world evidence.

Read the detailed description

Objectives Within-group changes in outcomes will be compared from baseline to the end of the study period.

Primary Outcome Measures:

Biomarkers in blood, measured using the Olink Target 48 Cytokine panel:

Tumor Necrosis Factor (TNF) Interleukin-1 Beta (IL1B) Interleukin-8 (CXCL8) Vascular Endothelial Growth Factor A (VEGFA)

Secondary Outcome Measures:

Remaining biomarkers in the Olink Target 48 Cytokine panel 36-Item Short Form Health Survey (SF-36) Frailty Index for Elders (FIFE) Depression Anxiety Stress Scale-21 (DASS-21)

Side effect profile including:

Number, type, severity, causality, and outcome of adverse events or unanticipated problems

Symptoms of aging, assessed by:

Aging Male Symptom scale Aging Female Symptom scale

Participant Details:

Study Duration per Participant: 7 days Total Number of Participants: 40

02

Conditions studied

  • Inflammation

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Keywords

  • Senolytic
03

In context

Inflammation

3,536 studies on the registry are indexed under Inflammation; 642 are open to participants now.

This study's planned enrollment of 40 is below the median of 50 across 2,577 interventional studies indexed under Inflammation.

Browse Inflammation studies →

Lead sponsor

Qualia Life Sciences is the lead sponsor of 14 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 79 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Provide voluntary, written, to participate in the study
  • Agree to provide a valid cell phone number and are willing to receive communications through text.
  • Healthy adults 45 - 79 years of age Can read and write English
  • Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly.
  • Willing to self-administer the fingerstick test kit at home for both a baseline and post-intervention blood sample, and to complete a release form that gives NHC access to the results of these tests.
  • Willing to complete questionnaires, records, and diaries associated with the study.

Exclusion criteria

Exclusion Criteria:

  • Women who are pregnant, breastfeeding, or planning to become pregnant during the trial
  • Known food intolerances/allergy to any ingredients in the product
  • Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, cancer
  • Having had a significant cardiovascular event in the past 6 months
  • Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines
  • On therapy
  • Individuals who were deemed incompatible with the test protocol
  • Adults lacking capacity to consent
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Active comparator
    Qualia Senolytic

    Dietary Supplement: Qualia Senolytic

Interventions

  • Dietary supplementQualia Senolytic

    Qualia Senolytic manufactured by Qualia Life Science

06

What researchers measure

Primary outcomes

  1. Olink Target 48 Cytokine panel - TNF, IL1B, CXCL8, VEGFA

    Biomarkers in blood, measured using the Olink Target 48 Cytokine panel: Tumor Necrosis Factor (TNF) Interleukin-1 Beta (IL1B) Interleukin-8 (CXCL8) Vascular Endothelial Growth Factor A (VEGFA)

    Time frame: 1 week

Secondary outcomes

  1. Remaining biomarkers in the Olink Target 48 Cytokine panel

    Time frame: 1 week

  2. 36-Item Short Form Health Survey (SF-36)

    Time frame: 1 week

  3. Frailty Index for Elders (FIFE)

    Time frame: 1 week

  4. Depression Anxiety Stress Scale-21 (DASS-21)

    Time frame: 1 week

  5. Aging Male/Female Symptom scale

    Time frame: 1 week

  6. Side effect profile as measured by a custom Safety and Tolerability survey

    Number of participants with treatment-related adverse events as assessed by a score of 3 or greater on the Safety and Tolerability survey

    Time frame: 1 week

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06953518
Responsible party
Sponsor
First posted
May 1, 2025
Start date
May 12, 2025 (estimated)
Primary completion
May 18, 2025 (estimated)
Completion
May 18, 2025 (estimated)
Last update
May 1, 2025

Study contacts

William Scuba
Contact
support@qualialife.com
855-281-2328

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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Discussion

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