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Aptuit

Aptuit, an Evotec company, is a pharmaceutical services provider that offers the most complete set of integrated early discovery to mid-phase drug development solutions by applying scientific excellence, outstanding service and a team of some of the foremost scientific professionals in the industry. These drug discovery and development professionals offer proven experience in key therapeutic areas. They share a legacy of success, having advanced a large number of molecules efficiently, expeditiously and economically, from early discovery through clinical development with low attrition rates. It is our uncommon expertise that allows Aptuit to identify the unexpected, mitigating risks and maximizing promising possibilities, ensuring exceptional results through an open, transparent climate of trust that our clients can count on. Our set of services include Drug Design & Discovery, API Development and Manufacture, Solid State Chemistry, CMC, and Preclinical and IND enabling GLP/GMP programs. Fully integrated drug discovery and development services are available from our facilities in the US and Europe.

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Pharmaceutical Manufacturing 717 Employees Found 8250 Similar Companies
717 Employees Found
96% Email Coverage
$300.0M Est Revenue
3 Office HQ
8250 Similar Companies
Sep '26 Last Verified

Aptuit Technology Stack

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Marketo

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Frequently asked questions about Aptuit

Who are the decision makers in Aptuit?

The decision makers in Aptuit are Leslie Patmore, Jeffrey Wilson, Maurizio Denaro, etc. Click to Find Aptuit decision makers emails.

What types of services does Aptuit offer for drug development?

Aptuit provides a comprehensive range of services that cover the entire drug development process from early discovery to mid-phase development. Their offerings include CMC (Chemistry, Manufacturing, and Controls), API (Active Pharmaceutical Ingredient) development and manufacture, drug design and discovery, preclinical and IND enabling GLP/GMP programs, and preclinical biosciences. They also specialize in solid-state chemistry and abuse liability testing, ensuring that clients have access to a complete suite of integrated solutions.

How does Aptuit support pharmaceutical companies in the early stages of drug discovery?

Aptuit supports pharmaceutical companies in the early stages of drug discovery by providing expertise in drug design and discovery, which includes target identification, lead optimization, and formulation development. Their scientific teams work closely with clients to develop tailored strategies that enhance the likelihood of successful drug candidates. Additionally, Aptuit's solid-state chemistry services help optimize the physical properties of drug compounds, which is crucial for their efficacy and manufacturability.

What is the INDiGO program offered by Aptuit?

The INDiGO program is a unique offering by Aptuit designed to streamline the path to Investigational New Drug (IND) application submission. This program integrates various services, including preclinical development, regulatory support, and CMC, to provide a cohesive strategy for clients. By leveraging Aptuit's scientific expertise and regulatory knowledge, clients can navigate the complexities of drug development more efficiently and effectively, reducing time to market.

What industries does Aptuit serve?

Aptuit primarily serves the pharmaceutical and biotechnology industries. Their clients range from large pharmaceutical companies to small biotech firms, all seeking to advance their drug development projects. Aptuit's expertise in various therapeutic areas, combined with their comprehensive service offerings, makes them a valuable partner for organizations looking to bring innovative therapies to market.

Can Aptuit assist with regulatory submissions and compliance?

Yes, Aptuit can assist clients with regulatory submissions and compliance. Their team includes experts familiar with the regulatory landscape, including the requirements for IND submissions and other regulatory filings. They provide guidance on GLP/GMP compliance, ensuring that all preclinical and clinical data meet the necessary standards for regulatory approval. This support helps clients navigate the complexities of regulatory processes and increases the likelihood of successful submissions.

What is abuse liability testing, and why is it important?

Abuse liability testing is a critical evaluation process that assesses the potential for a drug to be misused or abused. Aptuit offers this testing to help clients understand the safety profile of their drug candidates, particularly for those that may have psychoactive effects. This testing is important as it informs risk management strategies and regulatory submissions, ensuring that potential abuse risks are adequately addressed. By identifying and mitigating these risks early in the development process, Aptuit helps clients enhance the safety and marketability of their products.