Human therapeutic agents

a human therapeutic agent and chemotherapeutic technology, applied in the field of human therapeutic agents, can solve the problems of cancer death among women in low-income countries, cellular repair mechanisms to be less effective, and over-all risk accumulation, and achieve the effect of boosting psa counts

Inactive Publication Date: 2016-04-21
IONS PHARMA SARL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0027]A “chemotherapeutic” or “chemotherapeutic agent” as used herein refers to the combinations of chemical compounds described herein as useful in the treatment of human conditions, especially human cancers. Chemotherapeutics may be cytostatic, selectively toxic or destructive of cancerous tissue and/or cells, but also include indiscriminately cytotoxic compounds used in cancer treatments.
[0028]The combination ther

Problems solved by technology

Metastases are the major cause of death from cancer.
The overall risk accumulation is combined with the tendency for cellular repair mechanisms to be less effective as a person grows older.
Cervical cancer, which is caused by HPV, is a leading cause of cancer death among women in low-income countries.
In high-income countries, tobacco use, alcohol use, and being overweight or obese are major risk factors for cancer.
All of these techniques have significant drawbacks in terms of side effects and patient discomfort.
This can result in pain, diarrhea, constipation, mouth sores, hair loss, nausea, and vomiting.
During chemotherapies involving multiple-drug treatments, adverse drug events are common, and indeed toxicities related to drug-drug interactions are one of the leading causes of hospitaliza

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0229]In this example, the preferred GZ17-6.02 product was tested with two different human head and neck cancers (HN5 and OSC19), in order to determine the extent of cell death induced by the product.

[0230]Methods

[0231]The respective cells were individually cultured in a growth medium prepared using RPMI-1640 medium containing 11.1 mM D-glucose with 10% fetal bovine serum, 10 mM HEPES, 2 mM L-glutamine, 1 mM sodium pyruvate, 0.05 mM 2-mercaptoethanol, and Antibiotic-Antimycotic. These cells were maintained in T75 tissue culture flasks in a humidified incubator at 37° C. and 5% CO2. The media were changed on a third day after cell plating, and the cells were passaged on day 5 by trypsinization.

[0232]Formation of Cancer Spheroids

[0233]Custom-made micromolds with 100 um diameter wells were loaded with the cells (U.S. Pat. No. 8,735,154, incorporated by reference herein). The media were changed every day by partial replacement. Cell aggregates were allowed to form in the micromolds for ...

example 2

[0237]In this example, GZ17-6.02 was found to induce significant cancer cell death in human pediatric leukemia cells and pediatric osteosarcoma in a dose-dependent manner.

[0238]Jurkat leukemia cells were grown in suspension in media (RPMI supplemented with 10% FBS), maintained at approximately 500,000 cells / mL. The cells were plated in 96-well plates, and each well was exposed to a selected dose of GZ17-6.02 for 24 hours (a minimum of 4 replicates for each dosage). These cells were not treated to generate spheroids, but were directly plated onto the well plates. After a 24 hour exposure to the selected dosages of GZ17-6.02, PrestoBlue (Life Technologies, Inc) was added to each well and fluorescence readings were taken 4-6 hours later with an excitation wavelength of 485 nm and an emission wavelength of 560 nm, using a microplate reader (Enspire Multimode, PerkinElmer). Results were averaged following background subtraction and normalized to untreated cell controls.

[0239]Human osteos...

example 3

[0241]In this example, the effect of increasing doses of GZ17-6.02 in killing human lymphoma cells (mo205) and human lung cancer cells (H358) was tested.

[0242]The lymphomas treatment methods used were identical to those described in Example 2 relative to the pediatric leukemia cells, whereas the lung cancer treatment method was the same as described in Example 1.

[0243]FIGS. 3A and 3B set forth the results of these tests, and demonstrate the effectiveness of GZ17-6.02 in inducing lymphoma and lung cancer cell death.

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Abstract

Human therapeutic treatment compositions comprise at least two of a curcumin component, a harmine component, and an isovanillin component, and preferably all three in combination. The agents are effective for the treatment of human conditions, especially human cancers.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims the benefit of two Provisional Applications, Ser. No. 62 / 066,686, filed Oct. 21, 2014, and Ser. No. 62 / 161,090, filed May 13, 2015, each of which is incorporated by reference herein in its entirety.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention relates to combination chemotherapeutics for treatment of humans, and especially for the treatment of human cancers, and corresponding methods for the treatment of humans suffering from cancers or other maladies. The invention further provides dosage forms and regimens for administration to human patients, and methods of formulating and administering such dosage forms to yield improvements in treatment outcomes. More particularly, the invention is concerned with the administration of specific chemotherapeutic dosage forms (e.g., liquid mixtures, capsules, pills, or tablets) containing one or more curcumin component(s), harmine component(...

Claims

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Application Information

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IPC IPC(8): A61K31/12A61K31/11
CPCA61K31/11A61K31/12A61K31/192A61K31/437A61K31/4375A61K2300/00
Inventor ZAID, GENE H.BURGOYNE, THOMAS W.
Owner IONS PHARMA SARL
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