Designed Antimicrobial Peptides for Topical Treatment of Antibiotic Resistant Acne Vulgaris

SAN FRANCISCO, CA. – Riptide Bioscience, Inc., announces that key results from the application of its antimicrobial drug candidates for inflammatory acne vulgaris infections have been published in the journal Antibiotics, in an article titled ‘Designed Antimicrobial Peptides for Topical Treatment of Antibiotic Resistant Acne Vulgaris.’

Acne vulgaris, caused by the Gram-positive bacterium Cutibacterium acnes, is a prevalent dermatologic condition with causes considerable cutaneous and psychological morbidity, affecting over 80% of all adolescents and young adults worldwide. Mild forms can be treated with topical antibiotics, with severe forms of inflammatory acne requiring the prolonged use of oral antibiotics resulting in the development of antimicrobial resistance. Current acne treatments present side effects such as erythema, scaling, burning, hair bleaching, bacterial resistance, and birth defects. Widespread application of small-molecule antibiotic treatments such as clindamycin has led to the evolution of resistant strains, such that many countries report that over 50% of strains are already resistant to antibiotics. So widespread is the problem that American Academy of Dermatology guidelines now recommend against monotherapy with currently approved antibiotics, to avert the further proliferation of resistant strains.

Riptide scientists have developed innovative topical treatment alternatives which, once clinically translated, can potentially provide complete microbicidal eradication with minimal safety issues and limited susceptibility to microbial resistance. ‘For several years we have been engaged in a systematic program to develop antimicrobial peptides which can be administered topically,’ reported Riptide’s Chief Scientific Officer, Dr. Jesse Jaynes. ‘These are rationally engineered analogs of naturally occurring peptides that provide the first line of defense against invading pathogens in all multicellular organisms.’

Study co-author Dr. L. Edward Clemens continued, ‘These peptides show greatly improved efficacy compared with presently used acne treatments. Just as important, they kill acne pathogens upon contact by disrupting the cell membrane, giving the bacteria no opportunity to mutate so as to evolve resistant strains. That’s different from current treatments. The current antibiotics generally are non-lethal. Instead they attempt to interfere with reproduction over many hours, and do so only through biochemical pathways which the bacteria can evolve to circumvent.’

Riptide’s leading designed antimicrobial peptides demonstrated potent broad-spectrum activity against antibiotic resistant strains of C. acnes. They were active against clindamycin resistant isolates, active against tetracycline resistant isolates, and active against erythromycin resistant isolates. The peptides are bactericidal and selectively kill the causative C. acnes microorganisms via an immediate and direct pathogen membrane-lytic mechanism, while leaving mammalian cells unharmed. This unique mechanism has a reduced likelihood of developing bacterial resistance.

The lead peptide, RP556, was evaluated further in a multidrug-resistant C. acnes intradermal murine infection model: the peptide eliminated C. acnes infection following topical application, with no adverse treatment related effects observed. Dr. Clemens concluded, ‘The results with RP556 are very encouraging. If these results are clinically translated, designed antimicrobial peptides may serve as an important therapy for the topical treatment of recalcitrant acne infections.’

The open access paper entitled: ‘Designed Antimicrobial Peptides for Topical Treatment of Antibiotic Resistant Acne Vulgaris’ is available at https://www.mdpi.com/2079-6382/9/1/23

Riptide Bioscience, Inc., with laboratories in Vallejo, California, maintains an intensive program of research into peptide-based therapeutics. Contact: info@riptidebio.com

04 — News & Updates

Latest from Riptide.

Riptide’s programs are supported by a growing body of peer-reviewed publications and independent academic validation. Riptide has won substantial support through competitive grants from multiple National Institutes of Health (NCI, NIDDK, NEI, NIAMD), the US Department of the Army, Scleroderma Research UK, and private foundations.

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March 2, 2026

STANFORD, CA. – A collaborative study by US and Brazil scientists has demonstrated potent activity by Riptide’s RP557 among fungal pathogens designated as high priority by the World Health Organization. Writing in Microbiology, a team led by Dr. David Stevens of Stanford University and Dr. Melissa Xavier of the Mycology Laboratory, Federal University of Rio […]

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June 10, 2025

BIRMINGHAM, AL. – Researchers at the University of Alabama Medical Center have shown that radiolabeled versions of Riptide immune-modulating peptides can quantify immune responses in diabetes and cancer, potentially helping to drive treatment decisions. Obesity is a chronic inflammatory condition associated with diabetes, cancer, and cardiovascular disease. Over two-thirds of US adults are estimated to […]

Contact Riptide Bioscience

Riptide Bioscience welcomes inquiries from potential partners, licensees, and investors interested in our development programs and proprietary drug candidates. To explore collaboration or investment opportunities, please contact us at info@riptidebio.com.

Dr. Donald Kennedy†

Founding Advisor · In Memoriam

Prior to his untimely passing, Dr. Kennedy was a founding advisor and shareholder in Riptide Bioscience, and we strive to maintain the scientific rigor and higher objectives he inspired.  Dr. Kennedy was a noted neurobiology research scientist prior to chairing Stanford University’s Department of Biology and founding its Program in Human Biology.  He went on to serve as the US FDA Commissioner, later returning to Stanford as provost and ultimately University President.  Subsequently he served as editor-in-chief of Science.

Dame Carol Black

Board of Advisors

Dame Carol Black is a world-renowned expert in rheumatology, who served as Medical Director of the Royal Free Hospital at University College London, where she established Europe’s largest center for both scleroderma research and treatment.  Later she served as President of the Royal College of Physicians, and served as the UK government’s National Director for Health and Work.  She is co-president of the UK government organization focusing on the consequences of musculoskeletal disorders, and led the government’s Independent Review of Drugs.

Dr. Frank McCormick

Board of Advisors

Dr. Frank McCormick is among the world’s top cancer researchers, and received the first Stephenson Global Prize for his groundbreaking cancer discoveries.  Dr. McCormick’s pioneering work uncovered how mutations in the KRAS gene, present in more than 90% of pancreatic ductal adenocarcinomas (PDAC), disrupt the body’s natural ability to regulate cell growth. His discoveries have been foundational to the development of therapies targeting KRAS, a goal once thought unattainable.

Dr. Leonard Post

Board of Directors

Dr. Leonard Post has more than 30 years of experience with all stages of drug development, from early discovery through FDA approval.  Previously he served as Senior Vice President of Research and Development at Onyx Pharmaceuticals from 2000 to 2006. In this role, he was responsible for the co-development of Nexavar through to FDA approval for renal cancer. Onyx was sold to Amgen for $10 billion. Subsequently he served as Chief Scientific Officer and Co-Founder of LEAD Therapeutics (sold to BioMarin for $100M), and remained at BioMarin as Chief Scientific Officer.

Dr. Clayton Yates

Principal Scientist

Dr. Yates, Professor of Oncology, Pathology and Urology at Johns Hopkins University, has administered numerous grant awards from the National Cancer Institute and the Congressionally Directed Medical Research Program at the Department of Defense, and is a frequent invited speaker at national and international conferences focusing on prostate and breast cancer. Dr. Yates’ research focuses on how the tumor microenvironment influences epigenetic regulators, which can cause tumor cells to undergo epithelial to mesenchymal transition (EMT), and promote metastasis.

Dr. L. Edward Clemens

Principal Scientist

Dr. Clemens is a biologist and pharmacologist with 35 years’ experience in drug development, including the first identification of antagonists useful for controlling estrogen-dependent cancers. Dr. Clemens has led research teams at companies including Parke-Davis, Scios, and Metabolex, including the team that prepared data for the IND and ultimate approval of a recombinant form of human natriuretic peptide for congestive heart failure.

Dr. Jesse Jaynes

Principal Scientist

Dr. Jaynes is a leading biochemist specializing in peptide design, and has served as Chief Scientific Officer at two previous companies. As documented in >120 peer-reviewed publications and >60 patents, the Jaynes Lab was first in the world to demonstrate antiprotozoal, plant disease resistance, and anticancer activity for designed lytic peptides both in vitro and in vivo. In agriculture, Dr. Jaynes’ antimicrobial peptides have been licensed by US Sugar / Tropicana for use in citrus crop protection.

Kathryn Woodburn, Ph.D.

Senior Vice President, Translational Sciences

Translational development executive with 25+ years driving programs from discovery through IND, clinical development, and regulatory approval. Known for shaping development strategy, integrating cross‑functional scientific disciplines, and delivering registration‑ready data packages. Career includes leadership roles at Life Edit Therapeutics (ElevateBio), Avalanche/Adverum (acquired by Eli Lilly), Affymax, and Pharmacyclics (AbbVie), complemented by a consulting practice supporting translational drug development, and regulatory strategy across gene therapy, gene editing, regenerative medicine, ophthalmology, pain, oncology, hematology, arthritis, inflammation, infection and drug delivery. Author of 70+ peer‑reviewed publications and inventor on 10 patents.

Henry Lopez, Ph.D.

EVP — Operations

Dr. Lopez is an executive with both hands-on and management expertise in preclinical development, focusing particularly on execution of a wide variety of in vitro and in vivo assays.  Dr. Lopez managed laboratories at Xoma, Glycomed, and ultimately Parke-Davis/Pfizer as Director of its Phenotyping Core.  He went on to found MuriGenics, a large Contract Research Organization, servicing publicly-held and privately-held pharmaceutical companies worldwide.  Dr. Lopez is also an Associate Professor at the Division of Medicine, University College London.

Charles Garvin

CEO

Mr. Garvin, a seasoned CEO and technology investor, has a BA and JD from Harvard University, and did PhD study at Oxford University as a Rhodes Scholar. He has been Chairman, CEO, or controlling shareholder at a number of tech and biotech companies during a 40-year career. Mr. Garvin served as an officer and member of the Board of Directors at the Boston Consulting Group, a leading strategy consulting organization, and was one of the original principals of the Beta Group, a seed capital firm which has incubated several successful medical technology companies. Subsequently Mr. Garvin has served as Chairman or represented controlling interests in companies of up to $350 million in revenues, including TVC Communications, Riviera Trading, EK Holdings and Basic Industries. He is currently a Director of Tosk, Inc. (cancer chemotherapies) and Senior Advisor to SanBio (stem cell therapies).