Daily Newsletter

12 September 2023

Daily Newsletter

12 September 2023

GARDP and Orchid Pharma enter antibiotic sublicence deal

Shionogi will provide the key data required for the production of the antibiotic to Orchid.

Vishnu Priyan September 12 2023

The Global Antibiotic Research & Development Partnership (GARDP) and Indian company Orchid Pharma have entered a sublicence agreement for the production of antibiotic cefiderocol for treating specific Gram-negative infections.

The latest agreement is a vital step under a project by Shionogi, GARDP and the Clinton Health Access Initiative (CHAI).

Unveiled in June 2022, the project is intended to offer this antibiotic to various low and middle-income countries, following necessary approvals.

It is aimed at eliminating the gaps in equal access to crucial antibiotics across the globe, especially for regions with greater antimicrobial resistance rates.

Under a licensing deal signed by Shionogi and GARDP last year, the latter delivers cefiderocol to 135 countries that do not have access to the antibiotic.

As per the new deal, CHAI will aid in the technology transfer process between Shionogi and Orchid while Shionogi will provide key data required for the production of the antibiotic to Orchid.

This approach will facilitate Orchid in manufacturing cefiderocol and cutting down expenditures that patients might have to bear otherwise. 

Cefiderocol received approvals from the US Food and Drug Administration and the European Medicines Agency in 2019 and 2020, respectively.

This antibiotic is also part of essential therapies under the World Health Organization’s list.

GARDP executive director Manica Balasegaram said: “We can effectively offset the burden of antibiotic resistance by reducing the access gap between high and lower-income countries so that the right antibiotics are affordable and available for appropriate use.

“We are proud to work with Orchid to help make this a reality for cefiderocol and we hope that this project can help pave the way for access to additional antibiotics in the future.” 

Significant opportunities and risks for disease-modifying therapies (DMTs) entering the PD market

As PD therapy currently centers on symptomatic treatment, the need for DMTs is one of the greatest unmet needs. Several companies within the late-stage PD pipeline are developing drugs that target PD via novel MOAs. KOLs remain hopeful that these companies will uncover a class of drugs that works effectively to slow or modify the disease course. Targeting α-synuclein and other neurotoxic proteins is a key strategy in the late-stage pipeline for DMTs.

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