Oncovista Innovative Therapies Inc
OTC:OVIT
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Eurotel SA
WSE:ETL
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Oncovista Innovative Therapies Inc
Non-Reccuring Items
Oncovista Innovative Therapies Inc
Non-Reccuring Items Peer Comparison
Competitors Analysis
Latest Figures & CAGR of Competitors
| Company | Non-Reccuring Items | CAGR 3Y | CAGR 5Y | CAGR 10Y | ||
|---|---|---|---|---|---|---|
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Oncovista Innovative Therapies Inc
OTC:OVIT
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Non-Reccuring Items
N/A
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CAGR 3-Years
N/A
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CAGR 5-Years
N/A
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CAGR 10-Years
N/A
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Abbvie Inc
NYSE:ABBV
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Non-Reccuring Items
-$5.9B
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CAGR 3-Years
-43%
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CAGR 5-Years
-20%
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CAGR 10-Years
-18%
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Gilead Sciences Inc
NASDAQ:GILD
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Non-Reccuring Items
-$1.8B
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CAGR 3-Years
24%
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CAGR 5-Years
21%
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CAGR 10-Years
N/A
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Amgen Inc
NASDAQ:AMGN
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Non-Reccuring Items
-$7.1B
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CAGR 3-Years
-144%
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CAGR 5-Years
N/A
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CAGR 10-Years
-61%
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Vertex Pharmaceuticals Inc
NASDAQ:VRTX
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Non-Reccuring Items
-$512m
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CAGR 3-Years
-59%
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CAGR 5-Years
N/A
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CAGR 10-Years
-72%
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Regeneron Pharmaceuticals Inc
NASDAQ:REGN
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Non-Reccuring Items
-$297m
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CAGR 3-Years
17%
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CAGR 5-Years
N/A
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CAGR 10-Years
-32%
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Oncovista Innovative Therapies Inc
Glance View
OncoVista Innovative Therapies, Inc. is a drug development company, which engages in the development and commercialization of targeted cancer therapies. The company is headquartered in San Antonio, Texas. The company went IPO on 2006-01-23. The firm is engaged in developing targeted anticancer therapies by utilizing tumor-associated biomarkers. The firm's product pipeline consists of advanced (Phase II) and early (Phase I) clinical-stage compounds, late preclinical drug candidates and early preclinical leads. The firm's therapeutic strategy is based on targeting the patient's tumors with treatments that will deliver drugs selectively based upon specific biochemical characteristics of the cancer cells comprising the tumor. The firm's products include: Cordycepin (OVI-123) and L-Nucleoside Conjugates (OVI-117). Cordycepin depends upon the presence of a DNA polymerase, known as terminal deoxynucleotidyl transferase (TdT), for its therapeutic activity. OVI-117 is a thymidylate synthase (TS) inhibitor with pharmacological properties, which results in a retention of efficacy and a reduction of toxicity.
