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Continuing Education Activity

Adapalene is a topical retinoid with FDA approval for the treatment of acne vulgaris. Clinicians use retinoids are used to treat a wide variety of skin disorders. Adapalene also has multiple off-label therapeutic applications, including the treatment of verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders, actinic keratoses, and alopecia areata. This activity outlines the indications, contraindications, interactions, monitoring, and other therapeutic information pertinent to members of an interprofessional team in the care of patients on adapalene therapy.


  • Identify the approved indications for adapalene.
  • Describe the mechanism of action of adapalene.
  • Summarize the adverse effect profile of adapalene.
  • Review interprofessional team strategies for improving care coordination and communication to improve outcomes for patients using adapalene.
Access free multiple choice questions on this topic.


Adapalene is a topical retinoid that is FDA-approved for the treatment of acne vulgaris. Like other retinoids, adapalene has been used off-label for a variety of skin conditions, including verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders such as melasma and post-inflammatory hyperpigmentation, actinic keratoses, and alopecia areata.[1][2][3] Additionally, adapalene and adapalene analogs are under investigation for potential anti-microbial, anti-cancer, and neuroprotective effects.[4]

Adapalene was initially FDA-approved in 1996 for acne in patients 12 years of age or older. The FDA-approved adapalene 0.1% gel as an over-the-counter acne treatment in patients 12 and older in 2016. Formulations of adapalene 0.1% lotion, cream, and 0.3% gel are available by prescription only.

Retinoids are vitamin A derivatives that are typically described in terms of generations with increased specificity of retinoic acid receptor (RAR) affinity with later generations. Adapalene is a third-generation synthetic retinoid developed to improve the side effect profile compared to tretinoin, a first-generation topical retinoid that more closely resembles natural vitamin A in structure.[4][5] Second-generation retinoids are oral medications. The primary representative of the second generation is acitretin, which has enhanced benefits to the skin but has limited therapeutic use due to the significant risk of toxicity and is contraindicated for people of childbearing potential.[6] Third-generation retinoids include adapalene, tazarotene, and bexarotene. Of the third generation, bexarotene is a synthetic retinoid that binds exclusively to retinoid X receptors (RXR). Adapalene and tazarotene have higher specificity for RAR-gamma and RAR-beta and do not interact with RXRs making them suitable for topical administration with minimal systemic absorption.[5][7][8] Trifarotene is a fourth-generation topical retinoid FDA-approved in 2019 for the treatment of acne with a 20-fold greater affinity for RAR-gamma, the most dominant subtype in the skin, and has no affinity for RXR receptors.[8]

Retinoids modulate epidermal growth and differentiation, stimulate humoral and cellular immunity, decrease the inflammatory response, and reduce cell proliferation. The diverse biological actions of retinoids make them ideal for treating a wide variety of skin disorders. [5][6]Topical retinoids are recommended as first-line therapy to treat acne vulgaris, either alone or in combination with other acne medications.[9] Topical retinoids used in the treatment of acne vulgaris include adapalene, tretinoin, tazarotene, and trifarotene. Topical retinoids target two pathogenic mechanisms of acne vulgaris: microcomedone formation, which is the precursor of all forms of acne lesions, and the inflammatory response.[7]

Conventional teaching indicates that the retinoids used to treat acne have varying degrees of efficacy and tolerability. Adapalene is perceived to be the least effective but the best tolerated. Tretinoin is understood to have moderate efficacy and tolerability. Tazarotene is perceived to be the most efficacious but the least tolerated due to skin irritation. Currently, conventional teaching does not yet compare trifarotene with prior generations; however, it has increased ability to induce gene expression compared to tazarotene.[8]

Despite these conventions, studies support that adapalene is efficacious in treating acne vulgaris compared to other retinoids. A meta-analysis including five randomized controlled trials suggested that adapalene 0.1% gel had similar efficacy but enhanced tolerability in acne treatment compared to tretinoin 0.025% gel.[8] Adapalene has also been compared to tretinoin in a vehicle formulation of microsphere gel, which allows for tretinoin to be delivered primarily to the epidermis with the effect of decreasing irritation and increasing tolerability. A randomized controlled trial of tolerability, safety, and efficacy of adapalene gel 0.1% and tretinoin 0.1% microsphere gel revealed that the efficacy was comparable in terms of total, non-inflammatory, and inflammatory lesions. However, the adapalene patient group exhibited significantly enhanced cutaneous tolerability.[5]

Adapalene also performs well when compared to tazarotene. In a 12-week randomized, evaluator-blinded study comparing adapalene 0.3% gel and tazarotene 0.1% gel, each group had a clinically significant reduction in total lesion counts. A 61% reduction in acne lesions occurred with the use of adapalene, with a 57% reduction in the tazarotene group. Adapalene, 0.3% gel, was found to have equivalent efficacy as tazarotene 0.1% gel. However, patients using adapalene experienced less irritation than patients in the tazarotene-treated group.[10]

Adapalene has additional advantages when compared to other retinoids. Adapalene is a more stable molecule, which leads to less concern for molecular photodegradation, allowing for use during daylight hours. This stability contrasts with both tretinoin and tazarotene, which are photolabile. The stability of adapalene allows for use in combination with benzoyl peroxide, which has a synergist effect. A randomized double-blinded study of topical adapalene 0.3%-benzoyl peroxide 2.5% demonstrated significantly greater efficacy in patients with moderate-to-severe inflammatory, non-nodulocystic acne. With the synergistic effect of benzoyl peroxide, adapalene 0.3% increases patient treatment options for moderate to severe acne.[2][4][11]

Mechanism of Action

Adapalene is a naphthoic acid derivative designed to be more structurally rigid than previous retinoid generations, which decreases its ability to bind multiple retinoid receptors, thus decreasing off-target effects. Adapalene is an active metabolite and therefore requires no metabolic conversion. The adamantane nucleus is the chemical moiety that allows for adapalene to attach to RAR-beta and RAR-gamma. This complex then binds DNA through retinoic acid response elements and induces gene transcription, leading to downstream keratinocyte proliferation and differentiation. As a result, adapalene decreases microcomedone formations, exfoliates mature comedones, and has anti-inflammatory effects.[4][5] Of note, the adamantane nucleus is a component found in multiple other drugs, including antivirals and anti-hypoglycemic agents. Adapalene and newer analogs are under investigation for new potential therapeutic uses due to the antiproliferative, antibacterial, and neuroprotective activity attributed to the adamantane moiety.[12][4]

The pathogenesis of acne vulgaris is multifactorial. The main factors associated with acneiform lesion development are follicular hyperkeratinization, sebum production by sebaceous glands, and inflammation. In acne-prone patients, keratinocytes accumulate in the lumen of the hair follicle due to increased keratinocyte proliferation and cohesiveness, leading to the formation of a keratotic plug, resulting in the microcomedone. The microcomedone is the precursor to all visible acne lesions like open comedones, closed comedones, inflammatory papules, pustules, and nodulocystic lesions. Adapalene normalizes the differentiation of follicular epithelial cells to prevent microcomedone formation. Adapalene, when applied topically, penetrates the hair follicles due to its lipophilic nature.

In addition to follicular hyperkeratinization, acne is also a disorder associated with inflammation. Propionibacterium acnes is a gram-positive, anaerobic rod found in the sebaceous follicle. P. acnes is present in both acne-prone individuals and those without acne. The hypothesis is that there may be differences in the strains of P. acnes or in the host response to P. acnes, which leads to its varying degrees of pathogenicity. P. acnes release mediators that contribute to comedone rupture and stimulate inflammatory cells. P. acnes stimulates the toll-like receptor II (TLR-2) pathway, which induces the release of pro-inflammatory modulators. This action leads to neutrophil recruitment and the release of enzymes that result in follicular epithelium rupture. One mediator, IL-12, promotes a TH1 immune response. Adapalene is thought to suppress polymorphonuclear lymphocyte chemotaxis and down-regulate 15-lipoxygenase and TLR-2, contributing to its anti-inflammatory effects. The anti-inflammatory action of adapalene is comparable to betamethasone-17-valerate and indomethacin.[5][7]


Adapalene is applied once daily, either in the morning or at bedtime, to a clean face. The patient should wash the face with a gentle cleanser and allow the face to dry thoroughly. Then a pea-sized amount of adapalene should be applied as a thin layer to the entire face. Care is necessary to avoid application to eyelids, lips, and mucous membranes. An oil-free moisturizer can be applied over adapalene to help decrease the risk of irritation. As there is a risk of photosensitivity with topical retinoids, the clinician should also recommend an oil-free sunscreen and warn the patient against excessive sun exposure.

One reason for treatment failure with topical retinoids is the initial skin irritation that occurs and maximizes in intensity by 2 weeks of treatment. This initial mild irritation can lead to the discontinuation of treatment.[13] There are several options for treatment regimens to decrease the initial irritation as the skin acclimates to daily use. Options include application every other day, short contact therapy, or choosing a different drug vehicle.[7]

An investigation in modulating treatment regimens with adapalene 0.1%-benzoyl peroxide 2.5% combination in the first 4 weeks demonstrated no difference in efficacy outcomes at 12 weeks. The treatment regimens investigated were topical nightly application, limited exposure application of 3 hours, every other night application, and nightly application with a gentle moisturizer.[7][11]

Adverse Effects

Adverse reactions reported from adapalene include photosensitivity, irritation, redness, dryness, itching, and burning. These are usually mild adverse events.[9][14]

Adapalene is less irritating compared to other topical retinoids. In a blinded, randomized, controlled, parallel-group study of 591 acne patients, a combined safety analysis conducted in the United States and Europe compared adapalene 0.1% gel and tretinoin 0.025% gel. The number of patients discontinuing the study due to adverse events was about twice as high in those using tretinoin (2.4%) compared to adapalene (1.3%). There were no systemic adverse reactions noted in the study. Most of the adverse reactions observed were related to skin irritation.[13] Multiple other studies have demonstrated similar findings.[5][7] Adapalene 0.1% and 0.3% have also been compared to tazarotene in multiple studies showing adapalene to be non-inferior in efficacy and demonstrated superior tolerability.[10][15] The enhanced tolerability of adapalene has been attributed, in part, to the selective affinity of adapalene to the nuclear RAR-beta and RAR-gamma receptors, as opposed to RAR-alpha. The decreased risk of skin irritation may contribute to better long-term compliance.[4]

Rare, severe allergic reactions characteristically demonstrate pruritus, facial edema, lip swelling, and/or eyelid swelling.[13][16] If a patient experiences anaphylactic reactions with symptoms, including facial swelling, hives, chest pain, or shortness of breath, adapalene should be discontinued, and the patient should seek immediate medical evaluation.


Contraindications include a history of hypersensitivity to adapalene or other retinoids. Relative contraindications include pregnancy, photosensitive disorder, eczema, sunburn, or concomitant use of other potentially irritating skincare products.


The patient should have a reassessment for efficacy in 12 weeks or sooner if severe adverse effects occur.

Adapalene was pregnancy category C under the prior FDA pregnancy classification system and should be avoided in pregnant patients. It is unknown whether adapalene is excreted in breast milk and thus requires caution in breastfeeding patients. Oral exposure of pregnant animals to high doses of third-generation retinoids resulted in retinoid embryopathies. Topical administration of adapalene results in minimal systemic absorption, with less than 0.01% absorbed systemically and clearance from plasma within 72 hours of application.[6][8][17][18]

The most sensitive adverse effect of retinoids is possible teratogenicity. Vitamin A is essential for embryo-fetal development. Both deficiencies and overabundance can disrupt normal development. First and second-generation retinoids are known to cause retinoid embryopathies with oral administration. Topically applied retinoids, including first-generation tretinoin, have minimal systemic absorption, and third- and fourth-generation retinoids are designed to minimize off-target effects. Concern for teratogenicity was first raised because of three reports to the FDA from 1986 to 1989 highlighting holoprosencephaly in infants exposed to topical retinoids in utero. Subsequent case series and observational cohorts did not corroborate the initial reports.[8] A recent systematic literature review and meta-analysis evaluating first-trimester exposure to topical retinoids demonstrated no clear increase in the risk of retinoid embryopathy.[6] However, the paucity of epidemiologic data is cause enough to approach the use of topical retinoids during pregnancy with caution. Topical retinoids are not currently recommended during pregnancy.[6][8][19]

Enhancing Healthcare Team Outcomes

Adapalene is a topical retinoid that is FDA-approved for the treatment of acne vulgaris and used off-label in the treatment of many conditions, including verrucae, molluscum contagiosum, Darier disease, Fox-Fordyce disease, Dowling-Degos disease, photoaging, pigmentary disorders such as melasma and post-inflammatory hyperpigmentation, actinic keratoses, and alopecia areata.

Clinicians (including mid-level practitioners) who prescribe this agent, as well as pharmacists interacting with patients, must be fully aware of its side effects and contraindications. Pharmacists will also perform thorough medication reconciliation. Due to the lack of epidemiologic data, clinicians should not prescribe adapalene to women during pregnancy or breastfeeding.[5][6][19] Dermatology specialty-trained nursing staff should be on hand to counsel and follow up with patients on adapalene therapy. Nursing should assess patient compliance, answer questions regarding dosing/administration, and monitor for adverse events and alert the prescriber promptly if present. Collaboration between all these disciplines in an interprofessional team can optimize adapalene therapy while minimizing adverse effects. [Level 5]

Review Questions


Stein Gold LF, Alexis AF, Harper JC, Tan JKL. Advances in Acne and Rosacea Therapy. Semin Cutan Med Surg. 2018 Jun;37(3S):S63-S66. [PubMed: 30192344]
Tan J, Bissonnette R, Gratton D, Kerrouche N, Canosa JM. The safety and efficacy of four different fixed combination regimens of adapalene 0.1%/benzoyl peroxide 2.5% gel for the treatment of acne vulgaris: results from a randomised controlled study. Eur J Dermatol. 2018 Aug 01;28(4):502-508. [PubMed: 30187864]
Bagatin E, Gonçalves HS, Sato M, Almeida LMC, Miot HA. Comparable efficacy of adapalene 0.3% gel and tretinoin 0.05% cream as treatment for cutaneous photoaging. Eur J Dermatol. 2018 Jun 01;28(3):343-350. [PubMed: 30105991]
Rusu A, Tanase C, Pascu GA, Todoran N. Recent Advances Regarding the Therapeutic Potential of Adapalene. Pharmaceuticals (Basel). 2020 Aug 28;13(9) [PMC free article: PMC7558148] [PubMed: 32872149]
Sardana K, Sehgal VN. Retinoids: fascinating up-and-coming scenario. J Dermatol. 2003 May;30(5):355-80. [PubMed: 12773802]
Williams AL, Pace ND, DeSesso JM. Teratogen update: Topical use and third-generation retinoids. Birth Defects Res. 2020 Sep;112(15):1105-1114. [PubMed: 32643315]
Chivot M. Retinoid therapy for acne. A comparative review. Am J Clin Dermatol. 2005;6(1):13-9. [PubMed: 15675886]
Kassir M, Karagaiah P, Sonthalia S, Katsambas A, Galadari H, Gupta M, Lotti T, Wollina U, Abdelmaksoud A, Grabbe S, Goldust M. Selective RAR agonists for acne vulgaris: A narrative review. J Cosmet Dermatol. 2020 Jun;19(6):1278-1283. [PubMed: 32100454]
Stein Gold L, Baldwin HE, Lin T. Management of Severe Acne Vulgaris With Topical Therapy. J Drugs Dermatol. 2017 Nov 01;16(11):1134-1138. [PubMed: 29141062]
Thiboutot D, Arsonnaud S, Soto P. Efficacy and tolerability of adapalene 0.3% gel compared to tazarotene 0.1% gel in the treatment of acne vulgaris. J Drugs Dermatol. 2008 Jun;7(6 Suppl):s3-10. [PubMed: 18575220]
Stein Gold L, Weiss J, Rueda MJ, Liu H, Tanghetti E. Moderate and Severe Inflammatory Acne Vulgaris Effectively Treated with Single-Agent Therapy by a New Fixed-Dose Combination Adapalene 0.3 %/Benzoyl Peroxide 2.5 % Gel: A Randomized, Double-Blind, Parallel-Group, Controlled Study. Am J Clin Dermatol. 2016 Jun;17(3):293-303. [PMC free article: PMC4863916] [PubMed: 26945741]
Wang C, Li H, Ma P, Sun J, Li L, Wei J, Tao L, Qian K. The third-generation retinoid adapalene triggered DNA damage to induce S-phase arrest in HaCat cells. Fundam Clin Pharmacol. 2020 Jun;34(3):380-388. [PubMed: 31808972]
Cunliffe WJ, Caputo R, Dreno B, Förström L, Heenen M, Orfanos CE, Privat Y, Robledo Aguilar A, Meynadier J, Alirezai M, Jablonska S, Shalita A, Weiss JS, Chalker DK, Ellis CN, Greenspan A, Katz HI, Kantor I, Millikan LE, Swinehart JM, Swinyer L, Whitmore C, Czernielewski J, Verschoore M. Clinical efficacy and safety comparison of adapalene gel and tretinoin gel in the treatment of acne vulgaris: Europe and U.S. multicenter trials. J Am Acad Dermatol. 1997 Jun;36(6 Pt 2):S126-34. [PubMed: 9204091]
Hayashi N, Akamatsu H, Iwatsuki K, Shimada-Omori R, Kaminaka C, Kurokawa I, Kono T, Kobayashi M, Tanioka M, Furukawa F, Furumura M, Yamasaki O, Yamasaki K, Yamamoto Y, Miyachi Y, Kawashima M. Japanese Dermatological Association Guidelines: Guidelines for the treatment of acne vulgaris 2017. J Dermatol. 2018 Aug;45(8):898-935. [PubMed: 29782039]
Pariser D, Colón LE, Johnson LA, Gottschalk RW. Adapalene 0.1% gel compared to tazarotene 0.1% cream in the treatment of acne vulgaris. J Drugs Dermatol. 2008 Jun;7(6 Suppl):s18-23. [PubMed: 18575222]
Weiss JS, Thiboutot DM, Hwa J, Liu Y, Graeber M. Long-term safety and efficacy study of adapalene 0.3% gel. J Drugs Dermatol. 2008 Jun;7(6 Suppl):s24-8. [PubMed: 18575223]
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Bookshelf ID: NBK482509PMID: 29494115


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