Drug Database
CL

clotrimazole + betamethasone (Flotiran / Lotrisone / Lotricomb)

✓ Approved

Merck & Co. · NR3C1 · Small Molecule

What is clotrimazole + betamethasone?

clotrimazole + betamethasone is a small molecule developed by Merck & Co.. It is approved for therapeutic indications via unknown.

Drug Profile

Brand NamesFlotiran, Lotrisone, Lotricomb
CompanyMerck & Co.
Drug ClassSmall Molecule
Molecular TargetNR3C1,
RouteUnknown
StatusApproved

Mechanism of Action

Molecular Targets

clotrimazole + betamethasone acts on 2 molecular targets:

NR3C1nuclear receptor subfamily 3 group C member 1 (GR, GCCR)
sterol demethylase, Candida albicans (ERG11)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

clotrimazole + betamethasone is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Infections and infestationsWound infection fungal✓ Approved

Related Research Articles

PubMedTrials2026-07-25

The World Health Organization Antenatal CorTicosteroids for Improving Outcomes in preterm Newborns (ACTION-III) trial-rationale for the selected lower steroid dose.

WHO ACTION Trials Collaborators

Antenatal corticosteroids (ACS), most commonly administered as betamethasone or dexamethasone, remain a cornerstone of care for women at risk of preterm birth. However, the standard 24-mg regimen introduced more than five decades ago has not undergone formal dose-finding evaluation. Emerging concerns regarding possible dose-related adverse effects, particularly among late preterm infants subsequently born at term, have renewed interest in optimizing corticosteroid exposure. Experimental data across species, supported by human pharmacokinetic analyses, indicate that fetal lung maturation is driven by sustained low corticosteroid concentrations rather than high peak levels. This commentary summarizes key experimental, pharmacokinetic, and modelling evidence that informed the selection of the lower-dose betamethasone phosphate regimen evaluated in the WHO ACTION-III trial and explains the scientific rationale for this dosing strategy. Pharmacokinetic modeling indicates that 2 mg betamethasone phosphate administered intramuscularly every 12 h for four doses achieves fetal concentrations within the 1 to 4 ng/mL range identified in experimental studies, while avoiding the supratherapeutic peaks observed with conventional regimens. The ACTION-III trial will evaluate whether this lower dose ACS regimen, chosen on the basis of carefully developed models and clinical studies, maintains clinical efficacy while potentially reducing unnecessary systemic corticosteroid exposure in women at risk of late preterm birth.Trial registration: ISRCTN11434567, registered on 7 June 2021.  https://www.isrctn.com/ISRCTN11434567?q=ACTION-III&filters=&sort=&offset=1&totalResults=1&page=1&pageSize=10 .

PubMedCureus2026-07-25

Economic Burden and Cost Differences Between Branded and Generic Topical Antifungals in India.

Dt Prateek P, Dongerkery Kavitha K, Deolekar Pradnya P, Dahibhate Atharva A et al.

India's pharmaceutical market is characterized by a significant presence of both generic and branded drugs, particularly for common ailments such as superficial mycoses (SFMs), which pose a substantial public health and economic burden. Patients in tropical countries like India, which have common superficial mycoses, need prolonged treatment because of their recurrence rates after initial treatment and due to incomplete therapy. Given the high variability in drug pricing and the imperative for cost-effective healthcare, a pharmacoeconomic analysis comparing generic and branded topical antifungals in India is crucial to inform prescribing practices and optimize resource allocation. The price comparison of various topical antifungal medications from different brands was conducted by using the latest information from the "Monthly Index of Medical Specialties" August to October 2025, and 1mg online pharmacy and Jan Aushadhi website. The study calculated the total expenses for 30 mL and 30 g dosage forms, which included cream, ointment, lotion, eye drops, and shampoo products of each drug brand. We conducted a comparison between different drug brands through their cost ratio, and percentage cost variation (PCV) analysis was done, keeping generic medicines prices (retrieved from the Jan Aushadhi website) as baseline values. The data analysis showed a significant variation in the costs of different brands of topical antifungals in the Indian market. After analysis, we identified itraconazole 1% ointment to have the highest cost variation at 8335.1%, followed by clotrimazole dusting powder (4740%). Ketoconazole 2% cream, bifonazole 1% lotion, and sertaconazole shampoo showed the smallest variation at 3.29%, 3.5%, and 11.3%, respectively. When generic and branded topical antifungals were compared, the highest cost variation was seen for clotrimazole 1% cream (3431.7%), and the least variation was observed for ketoconazole 2% powder (135.4%). When combination topical antifungals were compared, the highest percentage cost variation of 1479.4% was seen for clotrimazole 1%w/w and beclomethasone dipropionate 0.025%w/w cream, and the least percentage cost variation of 38.8% was seen for terbinafine (1% w/w) + ciprofloxacin (1% w/w) + metronidazole (1% w/w) + clobetasol (0.05% w/w). The market for topical antifungal agents demonstrates substantial price variation among available products. Regulatory authorities, pharmaceutical manufacturers, and clinicians must collaborate to achieve optimal reductions in drug costs. Strict implementation of cost regulation policies, along with increased awareness among clinicians regarding the rational selection of cost-effective therapies, is essential.

PubMedColloids and surfaces. B, Biointerfaces2026-07-25

Crosslinked hybrid micellar platform for targeted cutaneous drug delivery.

Thakur Neeraj S NS, Agrahari Vibhuti V, Kalia Yogeshvar N YN

Micellar systems are transformed upon contact with the stratum corneum lipids, disassembling and releasing their cargo. Thus, the development of micellar systems for sustained cutaneous delivery that retain structural integrity poses considerable challenges. Herein, a highly stable crosslinked hybrid micellar (cHy-Micelles) platform is developed for controlled cutaneous drug delivery. The amine functionalized N-(2-aminoethyl)pentacosa-10,12-diynamide (AMP-1) was synthesized first; then, hybrid micelles were prepared by mixing it with D-α-Tocopherol polyethylene glycol 1000 succinate (TPGS) using nanoprecipitation. The micelles were stabilized by UV light irradiation and then characterized to determine morphology, stability, and ability to deliver a cargo. The spherical cHy-micelles with < 50 nm size (37.84 ± 0.45 nm) were highly stable and monodispersed (polydispersity index 0.099 ± 0.004) in the final hydrogel formulation because of intermolecular crosslinking within the micelle. These cHy-micelles also showed excellent cutaneous retention ability and low skin permeation owing to the positive surface potential (ζ potential +42 ± 7.15 mV) - skin has an isoelectric point (pI) of 4-4.5. Interestingly, the targeted cutaneous delivery of poorly water-soluble rose bengal, itraconazole, and clotrimazole was achieved using the developed micelles without showing significant transdermal permeation. This new crosslinked hybrid micellar platform could have enormous potential for topical drug delivery since it could enable modified kinetics as compared to conventional micelles, whilst decreasing the risk of systemic side effects.

PubMedBiological trace element research2026-07-23

Health and Regulatory Assessment of Hydroquinone, Mercury and Steroids in Skin-Lightening Creams Marketed in Pakistan.

Shujait Mahnoor M, Nawaz Ch M M, Hussain Naqi N

People from all over the world use cosmetics to enhance their physical appearance, seeking social acceptance. Most locally produced skin-lightening creams used in developing countries are a mixture of fat and water applied to the skin surface. These Skin Lightening creams may pose a potential health risk due to their inclusion of various highly toxic active ingredients like hydroquinone, mercury, and steroids. This study quantifies the levels of these toxic substances in ten commonly used SLC brands in Pakistan and their associated health risks in samples marketed in Lahore. To determine the concentration levels of various ingredients, including hydroquinone, steroids (Betamethasone, Dexamethasone, Hydrocortisone, and Prednisolone), and mercury, high-performance liquid chromatography, ultra violet- high-performance liquid chromatography, and a direct mercury analyzer were used, respectively. Health risks were assessed by calculating Chronic Daily Intake (CDI) and Hazard Quotient (HQ). Results showed that some samples exceeded international limits for hydroquinone (up to 5.56%) and mercury (up to 4.9 ppm), surpassing U.S Food and Drug Administration (USFDA), Pakistan Standards and Quality Control Authority (PSQCA), and World Health Organization (WHO) standards. The analysis also revealed undeclared corticosteroids in several samples: betamethasone (0.6-1.8% in 30% of samples), dexamethasone (1.4-6.4% in 20% of samples), hydrocortisone (0.4-8.5% in 50% of samples), and prednisolone (0.3-1.6% in 30% of samples). These findings suggest the need for improved regulatory enforcement in developing countries along with enhanced monitoring of Pakistan's cosmetic industry to effectively protect public health from the cumulative toxicity of hydroquinone, mercury, and corticosteroids.

PubMedPakistan journal of medical sciences2026-07-23

Hand-Foot Syndrome as a Rare Side Effect of Bleomycin.

Hashmi Aateqa A, Abid Maryam M, Zafar Amjad A, Abbas Khokhar Muhammad M

Hand-Foot Syndrome is a rare adverse reaction to bleomycin-etoposide-cisplatin chemotherapy, characterized by acral skin desquamation, hyperpigmentation, and swelling involving the hands and feet. We report the case of a 32 years old Asian female, diagnosed with right-sided Stage-IV dysgerminoma, who developed cutaneous symptoms following the second cycle of chemotherapy. She presented with hyperpigmentation, swelling, and desquamation affecting both hands and feet. After consultation with the dermatology department, she was diagnosed with chemotherapy-induced skin toxicity. Bleomycin, along with other cytotoxic agents, was discontinued. Initiation of topical betamethasone therapy resulted in significant clinical improvement over the following weeks. One month after starting the treatment, her feet had healed completely, while her hands continued to improve in the recovery phase with ongoing supportive care. This case highlights a rare dermatologic complication of bleomycin-etoposide-cisplatin therapy, emphasizing the need for further exploration into its prevention and effective treatment strategies.

PubMedRecent patents on anti-cancer drug discovery2026-07-21

Uncovering the Underlying Mechanism of Clotrimazole against Ovarian Cancer by Transcriptomics and Experimental Investigations.

Wang Xin X, Wang Ning N, Liao Jiaqian J, Yang Guanghao G et al.

Ovarian cancer remains the most lethal gynecological malignancy globally. While Clotrimazole (CTZ) exhibits antitumor potential, its specific efficacy and mechanisms in ovarian cancer require elucidation. Proliferation and apoptosis were assessed in A2780 and SKOV3 cells using CCK-8, colony formation, and Annexin-V/PI assays. Mechanisms were explored via RNA sequencing, molecular docking, qRT-PCR, Western blotting, and immunofluorescence. In vivo efficacy and safety were validated using SKOV3 xenograft models. CTZ inhibited cell viability with 48-h IC50 values of 19.36 µM (A2780) and 46.01 µM (SKOV3). Apoptotic rates increased significantly to 48.4% and 20.3%, respectively. RNA-seq analysis identified 4,066 differentially expressed genes primarily enriched in the HER2/PI3K/AKT pathway. Experimental validation confirmed that CTZ significantly downregulated this pathway in vitro and in vivo. In xenograft tumor models, intraperitoneal CTZ administration reduced tumor volume by 48.68% compared to the vehicle group, with slight systemic toxicity. However, oral administration showed limited efficacy. It was found that CTZ inhibits ovarian cancer cell proliferation and induces apoptosis via the HER-2/PI3K/AKT signaling pathway. CTZ may bind to HER-2 and accelerate HER2 protein degradation. The Intraperitoneal administration of CTZ exerts potent in vivo antitumor effects, suggesting that future research should utilize novel drug delivery systems to improve oral bioavailability. CTZ is a promising therapeutic agent and may serve as a novel potent agent for ovarian cancer treatment. Its antitumor effects are at least partially mediated via the inhibition of the HER-2/PI3K/AKT signaling pathway.

+9017 more articles available with a free account

Sign up free to view all articles →

Ask about clotrimazole + betamethasone