>
Tiger Woods GOES NUCLEAR After Caitlin Clark BREAKS Guinness Record At RSM Classic
2026-10-28 -- Ernest Hancock & Professor James Corbett - MP3&4
Oman calls for Gulf, Iraq and Iran to unite under one security pact
Israeli Media: Saudi Arabia Offered Ansar Allah $1 Billion for Yemen Ceasefire
Ancient Builders Moved Stones We Still Struggle to Explain
Startup Unveils "Big Iron" Rocket Whose Upper Stage Is An Orbital Data Center
The NYPD's New Cell Tracker Is Built For Mobility
Electronic skin instantly displays touch as light
$10k EV hatch packs in 5-minute flash charging
Apex Recordhunter electric drone sets unofficial speed record
Space-age manna: USAF & SpaceX drop survival kit from orbit
World's first nuclear fusion power plant coming to WA | FOX 13 Seattle
Advanced Small Modular Reactors (SMRs)
A U.S. energy startup has demonstrated a new type of nuclear reactor that uses existing nuclear...

84.4% of cancer patients taking ivermectin + mebendazole for 6 months reported either CANCER DISAPPEARANCE, TUMOR REGRESSION, or CANCER STABILIZATION.
The largest real-world human study to date evaluating ivermectin and mebendazole in cancer patients is now peer-reviewed and published in Anticancer Research—a major international oncology journal of the International Institute of Anticancer Research (IIAR), established in 1995.
Our study, "Real-world Clinical Outcomes of Ivermectin and Mebendazole in Cancer Patients: Results from a Prospective Observational Cohort," represents one of the most compelling clinical signals ever documented for repurposed anti-parasitic therapies in oncology.
In this prospective real-world clinical program evaluation, a diverse population of cancer patients (n=197) was prescribed compounded ivermectin–mebendazole, with each capsule containing 25 mg ivermectin and 250 mg mebendazole. Participants were followed for approximately six months using standardized digital surveys assessing cancer outcomes, medication adherence, and tolerability.
At approximately six months post-treatment initiation, we observed an 84.4% Clinical Benefit Ratio (CBR)—meaning more than four out of five patients reported either no evidence of disease (remission), tumor regression, or cancer stabilization.
Nearly half of all patients (48.4%) reported the strongest positive outcomes, including no evidence of disease (32.8%) or tumor regression (15.6%). An additional 36.1% reported disease stabilization, while only 15.6% reported progression.
Importantly, adherence was remarkably high, with 86.9% completing the initial prescription and 66.4% remaining on therapy at six months.
Side effects were predominantly mild and manageable, reported in 25.4% of patients (primarily gastrointestinal), with 93.6% of those experiencing side effects continuing treatment after minor dosing adjustments.
What makes these findings especially notable is that this was a heterogeneous, real-world cancer population—including patients with prostate, breast, lung, colon, liver, and many other malignancies, many of whom were also undergoing conventional therapies such as chemotherapy, radiation, and surgery.