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Nanoform sets a new near-term business target for 2021

The Pharma Data

The information in the press release is information that Nanoform is obliged to make public pursuant to the EU Market Abuse Regulation. This press release contains forward-looking statements, including, without limitation, statements regarding Nanoform’s strategy, business plans and focus. . +46 7686 650 11. 2 Proof of Concept.

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Nanoform launches technology for biologics and sets new near-term business target for 2021

The Pharma Data

The information in the press release is information that Nanoform is obliged to make public pursuant to the EU Market Abuse Regulation. This press release contains forward-looking statements, including, without limitation, statements regarding Nanoform’s strategy, business plans and focus. Finnish time. About Nanoform.

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New Phase 3 Data Show TAK-620 (maribavir), an Investigational Drug for the Treatment of Transplant Recipients with Refractory/Resistant Cytomegalovirus (CMV) Infections, Meets Primary Endpoint

The Pharma Data

Maribavir, an orally bioavailable anti-CMV compound, is the only antiviral agent presently in Phase 3 development for the treatment of post-transplant patients with CMV in SOT or HSCT. In transplant recipients, reactivation of CMV can lead to serious consequences including loss of the transplanted organ and, in extreme cases, can be fatal.

Drugs 52
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Synthesis-to-Clinic®: integrating isotopic labeling and human ADME to reduce time to clinic

Pharmaceutical Technology

This is due to the fact that the current Good Manufacturing Practice (cGMP) standards required for human studies involve a significant investment in infrastructure and quality systems in order to efficiently comply with all national and international regulations. What makes Quotient Sciences’ approach to these study types unique?

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The impact of AI and ML on the future of drug discovery  

Drug Discovery World

It contains structure-related data for more than 3 million compounds, over 5000 unique animal and human validation datasets, and physiological parameters of 196 different subject populations (different species, gender, strain, sub-strain) and counting.

Drugs 111
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XPhyto Announces Drug Formulation Strategy and 2021 Milestones Innovation to Impact

The Pharma Data

Each study is planned to be carried out over an approximately two-week period as an open label, randomized, crossover, two-period, two-sequence, single dose pilot study to assess the relative bioavailability of each product. SOURCE: XPhyto Therapeutics Corp. View source version on accesswire.com: [link].

Drugs 52
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Accurate dosing: How to achieve maximum precision with poor-flowing products

Pharmaceutical Technology

Safety issues must also be addressed, such as containment and potential ignition factors. Frewitt’s expertise also includes solutions to the API containment space, with both rigid and flexible isolators. [i]