Macrocyclic lactone
Approved for certain human parasite infections. Extensive preclinical cancer data; human oncology still early (trials, observation).
Read more →An overview of studies, registries and experience worldwide — Asia, Africa, Latin America, the Middle East and integrative traditions — not only the US/EU. Summaries in English; every source linked in the original.
All three are antiparasitic drugs under investigation for oncology drug repurposing. Evidence levels differ.
Approved for certain human parasite infections. Extensive preclinical cancer data; human oncology still early (trials, observation).
Read more →Used against worms in animals. Cell and animal studies show microtubule and metabolism effects. Few formal human cancer RCTs.
Read more →Approved human anthelmintic. Strongest formal tracks against cancer: Michigan case, Johns Hopkins preclinical + phase I, Egypt mCRC, etc.
Read more →Investigational overviews for stages I–II: what standard care involves, and how IVM/FBZ/MBZ appear in literature and registries. Not approved treatment — standard care with an oncologist always comes first.
Frame for reading the protocol pages: standard care, investigational tracks, questions for the oncologist.
Open protocols →Early disease, high curative potential with standard care; investigational adjuncts as conversation — not replacement.
Stage I →Often multimodal adjuvant plans; formal IVM/MBZ trials more often enroll advanced disease.
Stage II →| Level | Meaning | Examples on this site |
|---|---|---|
| A | Published RCT / phase II–III with outcomes | Patil 2022; Egypt mCRC MBZ |
| B | Phase I safety / prospective cohort | Gallia 2021; Hulscher 2026 |
| C | Case series / case reports | Michigan ACC; FBZ self-admin series |
| D | Cell / animal studies | Tang; Dogra; Bai (Hopkins) |
| E | Systematic or narrative review | Robalino; Chai; ReDO |
| R | Registry entry (ongoing/planned) | NCT05318469, NCT07487805, NCT01729260 |
Cells, animals, case reports, real-world and early human studies worldwide point in the same direction. Formal “negative” cancer RCTs are few and narrow — that is why you rarely hear them.
Hundreds of papers: growth inhibition, apoptosis, microtubules, glucose, immune activation, synergy with chemo/ICI.
Positive map →Michigan 19 mo; Hopkins OS 21 mo; Egypt mCRC; Hulscher cohort; ASCO PR; Tippens/case series.
USA →China, Korea, India, Latin America, Africa, integrative practice — not only one Western clinic.
World →Short list of the few formal limitations: see here.
Shared spaces + less routine deworming → more infection → sick pets → caregiver burden (owner exhaustion). Resistance is real but precise. Processes and sources under the Pets menu.
Michigan case (MBZ, 19 mo stability), Johns Hopkins phase I (median OS 21 mo), Cedars-Sinai IVM+ICI (1 PR interim), Florida ICONIC, Tippens narrative, etc.
WHO global parasite programs, Korean and Chinese research, Indian and Egyptian trials, Japanese toxicology, Latin American patient practice, Ayurveda/TCM context.
FBZ social phenomenon in Korea, IVM mechanisms from Chinese labs, Ōmura discovery, Indian phase II GBM.
Read more →WHO MDA, onchocerciasis, Loa loa safety, Egyptian mCRC RCT with mebendazole, patient-driven IVM use.
Read more →IVM/FBZ/MBZ are modern molecules — but they meet traditional and integrative practice in real life.
Read more →