Tracing the Scientific Breakthroughs Behind AKNETIDE®

AKNETIDE® R&D has been grounded over a decade of research from molecular discovery to clinical validation. Below is a snapshot of key scientific and regulatory milestones that demonstrate its journey from lab bench to real-world acne care efficacy.

2014

Inception of AMP

Inception of antimicrobial peptide discovery from nature and lab development

2019

Granted the world first ever AMP additive for animal nutrition and health

Granted the world first-ever antimicrobial peptide zootechnical additive for animal nutrition

2023

The cyclopeptide was discovered

AKNETIDE®, a novel antimicrobial cyclopeptide with potent inhibition against C. acne and S. aureus, was discovered

2024

First clinical study by SGS

The first-ever clinical study, with SGS Cosmetic Lab, was completed and demonstrated the significant efficacy of sensible acne level alleviation

2025

Multi-MOAs established and a strict hospital clinical study completed

Mechanism Elucidation: Multi-MOAs were established and proven by a leading cosmetic research institute

A double-blinded placebo-controlled Clinical Study in a world-famous Dermatology Hospital was conducted.

Scientifically proven and Dermatologist Endorsed evidences behind AKNETIDE®

Backed by 10+ years of rigorous consistent research of antimicrobial bioactive peptides, and recently validated by leading independent biochemical laboratories and top-tier dermatology hospital, AKNETIDE® harvested myriads of evidences, either of mechanism or of clinical studies, enables it deserving a worldwide breakthrough anti acne cosmetic ingredient designed for EFFICACY without bragging.

SGS Clinical Study

AKNETIDE® embedded prototype formula demonstrated potent efficacy in significantly alleviating volunteers’ acne conditions from black heads to papules in 7 days.

In-vitro Safety Studies

Skin irritation, phototoxicity, eye irritation, sensitization to skin were all tested NEGATIVE;  HaCaT MTT Toxicity data was given.

Published Studies and Patents

Scientific publications documenting AKNETIDE®‘s clinical findings and mechanism of action are currently in preparation for peer-reviewed journal submission.

Pre-publication data is available to qualified cosmetic manufacturers and researchers under NDA. 

Contact info@dermatide.net to request access.

Frequently Asked Questions

What clinical evidence supports AKNETIDE®?

AKNETIDE® has been evaluated in a 7-day double-blind clinical study conducted through SGS, a globally recognised testing institution. Results showed an 88.7% reduction in blackheads, 51.0% reduction in papules, and 16.3% overall reduction in total acne lesions. A hospital-based dermatology trial was completed in 2025 to further validate multi-mechanism performance.

Is AKNETIDE® safe for sensitive skin?

Yes. AKNETIDE® has undergone in-vitro safety assessments for irritation, phototoxicity, and sensitisation, all of which confirmed a favourable safety profile. It has received dermatologist-tested designation and is COSMOS-approved as a natural raw material — suitable for use in cosmetic formulations targeting sensitive and reactive skin types.

What is an antimicrobial cyclopeptide and how is it different from other anti-acne actives?

An antimicrobial cyclopeptide is a ring-structured peptide that mimics the body’s host defence mechanisms to selectively inhibit pathogenic bacteria. Unlike antibiotics or chemical actives, cyclopeptides work by disrupting bacterial membrane integrity without promoting antibiotic resistance. AKNETIDE® is derived from a natural cyclopeptide scaffold and is the first of its class developed for cosmetic acne applications.

Has AKNETIDE® been published in peer-reviewed journals?

Publication of AKNETIDE® ‘s clinical and mechanistic data in peer-reviewed journals is in progress. The foundational antimicrobial peptide research behind AKNETIDE® spans from 2014, with the first regulatory approval of a related AMP zootechnical additive in 2019. Scientific publications are expected to be available shortly — please contact info@dermatide.net for pre-publication data on file.

CLINICAL STUDY — KEY PARAMETERS
tudy type: Double-blind, controlled clinical study
Certification: SGS (Société Générale de Surveillance) — globally accredited testing body
Duration: 7 days
Measurements: Blackhead count, papule count, pustule count, total lesion count
Assessment: Standardised dermatological grading at baseline and day 7
Safety screens: In-vitro irritation, phototoxicity, and sensitisation assessments (all passed)
Status: Completed 2024

RESULTS AT DAY 7

Blackheads reduced:      88.7%

Papules reduced:         51.0%

Pustules reduced:        13.6%

Total acne reduced:      16.3%