Can ivermectin be used topically for skin cancer treatment in humans?

Checked on February 7, 2026
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Executive summary

Ivermectin shows repeated anticancer signals in laboratory studies—killing or slowing tumor cells and inhibiting metastasis in cell cultures and animal models—but there is no reliable clinical evidence that topical ivermectin treats skin cancer in humans, and major dermatology guidance advises against using it for that purpose [1] [2] [3]. Topical ivermectin is an approved, well-tolerated therapy for parasitic and inflammatory skin conditions, but approval for those uses is not the same as proof of efficacy against human skin cancers, and experts warn that doses that work in mice may be toxic in people and that pursuing unproven therapies risks delaying effective cancer treatment [4] [5] [6] [3].

1. Laboratory promise: multiple mechanisms, consistent preclinical activity

A substantial body of preclinical research has documented that ivermectin can inhibit cancer cell proliferation, induce apoptosis, block pro‑tumor signaling pathways such as PAK1 and WNT‑TCF, impair metastatic processes like neutrophil extracellular trap (NET) formation in melanoma models, and potentiate other anticancer drugs—findings described across systematic reviews and individual studies in cell lines and mice [1] [7] [2] [8] [9]. Those studies establish biological plausibility: ivermectin affects cell cycle control, mitochondrial function, autophagy and immune‑related mechanisms that could plausibly suppress tumor growth or metastasis in experimental systems [1] [10] [2].

2. The translational gap: petri dish and mouse results do not equal human efficacy

Despite robust preclinical signals, oncologists and reviewers caution that the concentrations successful in vitro or in mouse experiments often exceed what is safely achievable in humans, and that animal dosing that drives anticancer effects could be toxic to patients—an obstacle repeatedly flagged in clinical commentaries and expert interviews [6] [9]. Reviews and editorials emphasize that repurposing an FDA‑approved antiparasitic into a cancer drug requires controlled human trials to define safe, effective dosing, delivery route and combination strategies; the current literature has many hypotheses but lacks randomized clinical data for skin cancer specifically [9] [1].

3. Topical ivermectin: an approved dermatology tool, not an oncology therapy

Topical ivermectin 1% cream is approved and clinically used for rosacea, scabies and other parasitic or inflammatory dermatoses, with tolerability and clear application guidance in dermatology resources such as Memorial Sloan Kettering and dermatology reviews [4] [11] [5]. Those approvals and safety data are relevant to dermatologic practice but do not establish antitumor efficacy against basal cell carcinoma, squamous cell carcinoma or melanoma in humans; the evidence for cancer comes primarily from non‑topical preclinical models or systemic experiments rather than validated topical clinical trials for skin cancer [11] [1] [2].

4. Professional guidance and practical risk: do not substitute proven cancer care

Authoritative dermatology guidance explicitly warns against using topical ivermectin to treat skin cancer because of absent clinical evidence and the real risk that patients who choose unproven topical regimens may delay curative surgery, radiation or systemic therapy [3]. Oncologists reporting on ivermectin’s “wildfire” interest stress drug interactions, neurological toxicity at high doses, and the need for physicians to counsel patients that experimental lab results are insufficient to recommend off‑label topical use for cancer without clinical trials [6] [3].

5. Anecdotes, case reports and emerging interest that require rigorous follow‑up

There are isolated case reports and popular accounts claiming success with ivermectin (and other antiparasitics) against skin cancer, but these are low‑quality observational anecdotes that cannot substitute for controlled studies; some online compilations of case reports have appeared, yet they postdate and do not change the lack of randomized human data [12]. Scientific reviewers repeatedly call for carefully designed clinical trials to test whether topical or systemic ivermectin can safely reach therapeutic concentrations in human tumors and to define which tumor types, if any, might benefit [9] [1].

6. Bottom line

The current evidence does not support using topical ivermectin as a treatment for skin cancer in humans: laboratory and animal data are provocative and justify clinical research, topical formulations are safe for certain dermatologic indications, but no reliable clinical trials demonstrate efficacy against skin cancers, and professional societies recommend against substituting topical ivermectin for established, evidence‑based cancer treatments [1] [4] [3] [6].

Want to dive deeper?
What clinical trials are underway testing ivermectin or other macrocyclic lactones for melanoma or nonmelanoma skin cancers?
How do the doses and delivery routes of ivermectin used in mice compare to safe human exposures in pharmacokinetic studies?
What evidence-based topical treatments are recommended for early nonmelanoma skin cancers and when should patients seek surgical care?