Developing Antibody Drug Conjugate (ADC) therapeutics? Inotiv has mass spectrometry assays to quantify your ADC target protein in any sample type, including FFPE tissue, without antibodies. We have developed assays to 27 ADC targets for oncology and other therapeutic applications.
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How Differences Between Experimental IBD Models Can Impact Your Drug Development Program
Due to the current FDA concern and guidance on reducing the risk of Nitrosamine impurities in human drugs, there has been an increased industry need for testing of these impurities using the Bacterial Reverse Mutation (Ames) test. As Nitrosamines are not readily detectable by standard Ames methodologies, specifically cited in the Ames testing guideline (OECD 471), the need for a robust protocol better suited for this class of compounds is warranted.
May 4-7, 2025 Boston, MA Booth #207 At NBC, leading scientists will gather to present and debate innovative solutions, gain insight into new emerging trends, and collaborative oppo...
May 7-9, 2025 Newark, DE The Genetic Toxicology Association (GTA) is a tax-exempt educational and scientific organization that was founded in 1975 and in...
May 13-17, 2025 New Orleans, LA Booth #1412 Join the Inotiv team at the American Society of Gene and Cell Therapy’s (ASGCT) annual meeting, the premier event for professionals in g...
May 7, 2025 — Second quarter fiscal 2025 revenue increased 4.4% to $124.3 million — Year-to-date fiscal 2025 revenue de...
April 23, 2025 WEST LAFAYETTE, Ind., April 23, 2025 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”...
February 05, 2025 Enhanced liquidity by $27.5 million through the issuance of ...
How Differences Between Experimental IBD Models Can Impact Your Drug Development Program
Due to the current FDA concern and guidance on reducing the risk of Nitrosamine impurities in human drugs, there has been an increased industry need for testing of these impurities using the Bacterial Reverse Mutation (Ames) test. As Nitrosamines are not readily detectable by standard Ames methodologies, specifically cited in the Ames testing guideline (OECD 471), the need for a robust protocol better suited for this class of compounds is warranted.
May 4-7, 2025 Boston, MA Booth #207 At NBC, leading scientists will gather to present and debate innovative solutions, gain insight into new emerging trends, and collaborative oppo...
May 7-9, 2025 Newark, DE The Genetic Toxicology Association (GTA) is a tax-exempt educational and scientific organization that was founded in 1975 and in...
May 13-17, 2025 New Orleans, LA Booth #1412 Join the Inotiv team at the American Society of Gene and Cell Therapy’s (ASGCT) annual meeting, the premier event for professionals in g...
May 7, 2025 — Second quarter fiscal 2025 revenue increased 4.4% to $124.3 million — Year-to-date fiscal 2025 revenue de...
April 23, 2025 WEST LAFAYETTE, Ind., April 23, 2025 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”...
February 05, 2025 Enhanced liquidity by $27.5 million through the issuance of ...
How Differences Between Experimental IBD Models Can Impact Your Drug Development Program
Due to the current FDA concern and guidance on reducing the risk of Nitrosamine impurities in human drugs, there has been an increased industry need for testing of these impurities using the Bacterial Reverse Mutation (Ames) test. As Nitrosamines are not readily detectable by standard Ames methodologies, specifically cited in the Ames testing guideline (OECD 471), the need for a robust protocol better suited for this class of compounds is warranted.
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