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Before
After
*ChemoRT Started
*SeaCare Started
*SeaCare is a lower strength formulation compared to Immune 12.
About Pacific Marine

Pacific Marine Biotech (PMB) is a United States-based biotech company founded in December 2021 by Samuel Grant and Alan Temkin. Their team’s mission is to provide a safe and natural treatment solution for Glioblastoma, GBM and Gliomas that restores quality of life by securing future Therapeutic  Goods of Australia (TGA) and U.S. Food and Drug Administration approval for the investigational drug Immune12.

PMB's immediate objective is to recruit patients for the Australia Phase II Efficiency Trial who can potentially benefit from the trial.  Additionally, they want to create partnerships with leading healthcare institutions in the US for the purpose of conducting clinical trials on Immune12. They envision a future in which they can positively change the way cancer is treated, rewriting the narrative for thousands of cancer patients every year and for the betterment of communities around the world.

We have secured a phase 2 clinical trial in Australia, click the button below to fill out the trial interest form.

FILL OUT OUR GBM AUSTRALIA TRIAL INTEREST FORM
*Not located in Australia? The products used in the trial are available through the Cancer Wellness Clinic. You can visit their site here..

Dr. Janet Schloss, PhD

Dr Janet Schloss has a background as a naturopath and clinical nutritionist and completed her PhD at the School of Medicine, University of Queensland. Janet has worked extensively conducting clinical trials and has led one of the world's first trials on cannabis and brain cancer. In addition, Janet has had a private practice seeing patients for over 25 years. She has extensive knowledge of trial design, trial implementation, quantitative and qualitative research, in conjunction with extensive industry knowledge. She regularly presents at conferences in Australia and worldwide and, to date, has over 70 peer-reviewed journal articles.

Immune12 Clinical Trial

If any patients, caregivers, or healthcare providers who are based in Australia, would like more information or to pre-qualify for this clinical trial should fill out our Interest Form or contact our EBCI Clinical Research Coordinator and Patient Navigator, Shreya Prakash, at Shreya@EndBrainCancer.org or at 425-436-8688.

A Phase 2 clinical trial of Immune12 is currently enrolling patients with glioblastoma brain cancer to support marketing authorization in Australia, with study locations in New South Wales and Queensland (registered with the Australian New Zealand Clinical Trials Registry, ANZCTR). The trial is led by Chief Principal Investigator Dr. Janet Schloss, PhD, ND, and plans to enroll approximately 60 participants. This study will evaluate how feasible the treatment is for patients, including how well participants are able to stay in the study and follow the treatment plan. Researchers will also study certain biomarkers in the blood, including those related to the kynurenine pathway, which may help scientists better understand how the body responds to treatment. In addition, the trial will assess patients’ quality of life during treatment. Doctors will use MRI scans throughout the study to monitor how tumors respond to treatment using established brain tumor evaluation guidelines called Response Assessment in Neuro-Oncology (RANO). Tumor responses may be categorized as complete response, partial response, stable disease, or disease progression. Learn more about the clinical trial HERE.

IMMUNE12 is currently being evaluated by PMB for its potential to revolutionize cancer treatment in the areas of efficacy, safety and delivery. While current cancer treatments can be successful in extending life by several months, they are risky, not curative, and often have debilitating side effects. With its formulation, Immune12 is being evaluated for potential:

  • Effectiveness in lowering GBM tumor growth beyond the current standard of care (SOC)
  • Anti-cancer properties
  • Low negative side effects, especially as compared to the current SOC
  • Ability to administer in any environment, even at home
LEARN MORE
*Pacific Marine recently updated their projected timeline for US based clinical trials for Investigational Product Immune12 which will be done in association with their ongoing FDA reviews and approvals.

Why This Work Matters

These MRI comparisons illustrate meaningful outcomes observed. At Pacific Marine Biotech, our mission is to advance a safe, natural biologic approach that may help rewrite what is possible for patients facing some of the most aggressive cancers.
Before
After 36 Months
Diagnosed with Methylated 
Inoperable Glioblastoma
*SeaCare is a lower strength formulation compared to Immune 12.
Before
After 2 Months
Diagnosed Inoperable
*SeaCare is a lower strength formulation compared to Immune 12.
Before
After 15 Months
Diagnosed with Unmethylated Operable
*SeaCare is a lower strength formulation compared to Immune 12.
Before
After 15 Months
Diagnosed with Unmethylated Operable
*SeaCare is a lower strength formulation compared to Immune 12.

Changing The Way Cancer Is Treated.

ENDBRAINCANCER INITIATIVE | CHRIS ELLIOTT FUND

Enhancing patient outcomes by expanding FDA-approved treatment modalities and fueling research in the pharma/bio/life sciences, device & diagnostic industries and by closing the existing GAP from initial diagnosis to IMMEDIATE AND EXPANDED ACCESS to specialists, researchers, advanced & innovative treatments, clinical trials and critical care with the ultimate goal of improving patient outcomes through updating and improving WHO & NCCN Guidelines and clinical practices related to Standard of Care for brain cancer patients.

TAX ID:26-2185614
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