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As of 8:10 PM 08/17/15 All times are local (Market data is delayed by at least 15 minutes).

canopus biopharma inc (CBIA) Snapshot

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canopus biopharma inc (CBIA) Details

Canopus BioPharma Incorporated, a pharmaceutical research company, provides pharmaceutical products and assay methods to patients suffering from infectious, cancer, and addiction diseases. It also provides antivirals, radiation protection products, oncology products, bio-barcode assays, camelidae blood products, and neutraceutricals. The company was founded in 1996 as Canopus Corporation and changed its name in 2007. Canopus BioPharma Incorporated is based in Santa Monica, California.

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canopus biopharma inc (CBIA) Key Developments

Canopus BioPharma Inc. Announces Positive Results from an In-Vitro Live Ebola Virus Study

Canopus BioPharma Inc. announced that it has completed crucial research in confirming efficacy of a prescription drug: CB008 for Ebola Virus inhibition. Laboratories at the Texas Biomedical Research Institute in San Antonio Texas have demonstrated complete in-vitro inhibition of the live Ebola Virus strain Zaire at concentrations of CB008 that are achievable by oral administration. CB008 is only one of a family of prescription drugs which has been demonstrated by Canopus BioPharma to have potential in preventing Hemorrhagic syndrome and inhibiting Ebola Viral replication. CB008 is an in-house codename for a well-established prescription drug first approved by the FDA in the early 1980's for other medical indications. CB008 is an effective, safe treatment for Ebola Virus. Canopus BioPharma has signed a confidential agreement with a major pharmaceutical company who are reviewing the results and the possibility of expediting an Ebola non-human primate study. Following this, CB008 can progress to a human Ebola patient clinical trial in West Africa.

Canopus BioPharma Inc. Announces Results from Compassionate Study in Hepatitis C patients in China

Canopus BioPharma Inc. announced topline results from a Compassionate Clinical Trial in China, evaluating the twice daily oral administration of Mogroside IV (Mogrovir(TM)). Mogrovir(TM) is a Toll-like receptor agonist and stimulator of the patient's immune system. Mogrovir(TM) was administered orally in combination with Ribavirn (RBV), for the treatment of Genotype 1, treatment naive Hepatitis C (HCV) patients. The study showed a statistically significant result regarding the improvement of both liver function and increased blood platelet counts. A selection of patients in the trial also showed a statistically significant reduction in HCV viral-load levels, in the three month follow up period post-therapy. HCV Viral-load in these specific patients were approaching zero after a period of 180 days (90 days Mogrovir(TM) Treatment and 90 days follow-up). This fact confirmed the immune activation effects which are expected from the immune activation characteristics of Mogrovir(TM). Twenty eight patients were enrolled in the Canopus BioPharma study and all patients completed the study, without any toxicity or negative side-effects being documented. Compared to baseline, significant improvements were observed for patients in malaise, anorexia, food intake, abdominal distension and sleep at day 90 of the study. Canopus BioPharma is currently co-ordinating with study centres in Europe and the USA to duplicate the results observed from this Chinese study. Since Hepatitis C and the Dengue Virus are both members of the Flavivirus family, Canopus BioPharma has initiated discussions in Singapore and Thailand with the intention of commencing patient studies with Mogrovir(TM) alone for the treatment of Dengue viral infections in patients.


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