Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06567119

Preliminary Evaluation of the Safety and Tolerability of SPOT-mRNA01 Subcutaneously Administered in Healthy Subjects

This is a first-in-human, randomized, double-blind, placebo-controlled clinical study to evaluate the Safety and Tolerability of SPOT-mRNA01 injection in healthy adult volunteers.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

About this study

SPOT-mRNA01 (collagen 1 alpha 1 (COL1A1) mRNA-loaded by Extracellular vesicles (EVs)) can induce collagen protein grafts in dermal tissue, thereby supplementing collagen and reducing wrinkle formation in collagen-depleted skin. Therefore, SPOTmRNA01 can provide a source of human collagen intradermally for cosmetic anti-aging use.

This is a first-in-human randomized, double-blind, placebo-controlled, single-dose, dose ascending, exploratory clinical study to evaluate the Safety and Tolerability of SPOT-mRNA01 administered by subcutaneous injection to healthy adult volunteers.

Biopsies will be used to detect the expression of collagen in the skin of the injection area.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Aged 18 to 75 years inclusive at the time of informed consent.

Exclusion criteria

  • Any transient or chronic skin condition, disorder, or infection within 20 cm of the target areas before treatment that, in the opinion of the investigator, may confound study results.
  • History of laser treatment or chemical peels or any cosmetic anti-aging treatments to the target areas within six months of the study treatment.
  • History of surgical procedures to target areas, including removal of benign or malignant skin cancers that, in the opinion of the investigator, may confound study results.
  • Participant with a history of heavy smoking, alcohol or drug abuse or steroid treatment.
  • Pregnant or breast-feeding females.
  • History of anaphylaxis or allergic reactions to any constituent of the study product and/or local anesthetics, and/or history of severe abnormal drug reaction.
  • Those who have participated in clinical trials of other investigational drugs within 3 months before the study treatment.
  • Those who are not suitable for subcutaneous injection and biopsy.
  • Any condition that the investigator or primary physician believes may not be appropriate for participating the study.

Treatment and study plan

SPOT-mRNA01

Biological

SPOT-mRNA01 (COL1A1 mRNA-loaded by EVs) ,single-dose subcutaneous injection

Placebo

Other

Sterile isotonic solution, subcutaneous injection

Primary outcomes

  1. Assessment of the frequency and severity of AEs caused by SPOT-mRNA01

    Time frame: 3 months

    The investigator will collect a description of the events, time of onset and resolution, assessment of severity and causal relationship to SPOT-mRNA01.

Secondary outcomes

  1. level of COL1A1 protein expression in local dermal tissue after subcutaneous injection of SPOT-mRNA01

    Time frame: Days 4, 7 and 31

    Local collagen expression in injection area biopsy by ELISA detection

  2. Assessment of skin thickness after subcutaneous injection of SPOT-mRNA01

    Time frame: Days 4, 7 and 31

    Detecting local skin thickness in injection site biopsy by Masson trichrome stain.

  3. Assessment of skin thickness after subcutaneous injection of SPOT-mRNA01

    Time frame: Baseline and days 7, 15, 31, 61 and 91

    Detecting local skin thickness by Skin ultrasound.

Sponsors and collaborators

Lead sponsor

SIPO Biotechnology Co. Ltd.

Industry

Collaborators

  • Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled Exploratory Clinical Study to Evaluate the Safety and Tolerability of SPOT-mRNA01 Injection in Healthy Adult Subjects.

Important dates

Study start
2027
Primary completion
2029
Study completion
2029
First posted
Aug 22, 2024
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.