Here you’ll find timely and relevant information about our company, including press, and social media channels focusing on the development of tropical disease medicines for malaria prevention and dengue fever treatment.
Please join CEO Geoffrey Dow as he discusses future plans for testing of ARAKODA® (tafenoquine) for potential use in COVID-19 in light of recent in vitro study results.
60P attends the 10th Annual European Life Sciences CEO Forum (ELSCEO) as a presenter and a partnering company.
60P attends AusBiotech Series.
60P attends International Bio as a presenting and partnering company.
60 Degrees Pharmaceuticals Awarded U.S. Patent Covering Tafenoquine for Treatment of COVID-19 and Other Lung Infections
Positive Phase II Study Data for ARAKODA® (tafenoquine) in Patients with Mild-Moderate COVID-19 Disease Published by New Microbes and New Infections; Larger Studies Planned to Confirm ARAKODA Accelerates Clinical Recovery in Mild-Moderate COVID-19
Positive Phase II Study Data Suggest ARAKODA® (tafenoquine) Numerically Improved Clinical Recovery in Patients with Mild-Moderate COVID-19 Disease
ARAKODA® (tafenoquine) clinical safety, tolerability confirmed in long-term safety study; results published in Tropical Medicine and Infectious Disease
Data Safety Monitoring Board Recommends Completion of Phase II Study to Evaluate the Efficacy and Safety of ARAKODA® (tafenoquine) for Treatment of Mild-Moderate Covid-19 Disease
60 Degrees Pharmaceuticals Announces Completion of Long-Term Safety of ARAKODA® (tafenoquine) in Healthy Adult Volunteers
60 Degrees Pharmaceuticals Announces Positive Results of Cell Culture Testing of ARAKODA® (tafenoquine) for COVID-19
ARAKODA™ (tafenoquine) tablets, first prescription drug approved for malaria prevention by US FDA in over 18 years,
now available in US
60 Degrees Pharmaceuticals (60P) achieves first global product launch milestone
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KODATEF® (tafenoquine) approved in Australia; first malaria prevention drug in more than two decades
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Military scientists have discovered a new malaria drug that could help eradicate the disease — and it’s hitting shelves soon
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U.S. Food and Drug Administration Approves ARAKODA™ (tafenoquine) tablets for oral use
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U.S. FDA Advisory Committee votes in favor of Tafenoquine for the prevention of malaria
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Priority Review Designation Received for Tafenoquine
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60P received Priority Review Designation from the USFDA for Tafenoquine (TQ) for prevention of malaria in adults
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US Army Medical Research Lab Gets Fast Track Approval from USFDA for Malaria Drug
60 Degrees Pharmaceuticals Fast Tracked For Malaria Drug
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60P Submits New Drug Application to USFDA for Antimalarial Drug Tafenoquine
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60P’s investigational antimalarial agent tafenoquine is shown to be free of neurologic toxicity in adult rats according to recent study findings.
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60P has received the first tranche of $4 million in a debt financing deal with Knight Therapeutics Inc. in support of our drug development program for tropical diseases.
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60P has received approval to conduct a clinical study with celgosivir and modipafant in dengue patients in collaboration with Singapore General Hospital.
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60P recently entered into a cooperative research and development agreement with the US Army to commercialize 60P003 (Tafenoquine) for malaria prophylaxis.
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60P recently entered into an exclusive licensing deal with SingHealth and Duke-National University of Singapore Graduate Medical School to further develop celgosivir (60P001) for dengue fever.
One of 60P’s partners, Duke-NUS Medical School and its collaborators, completed a Phase I clinical study that demonstrated the safety of celgosivir in dengue patients and a trend toward faster NS1 clearance, suggesting the possibility of mitigating vascular permeability syndrome using glucosidase inhibitors.
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60P has entered into a research collaboration agreement with the Duke-NUS Medical School to investigate the utility of different combinations of dengue drugs. Dengue, like other viral diseases, will likely require a combination of different host and virus-targeted molecules to achieve useful clinical benefit. Studies performed by Dr. Subhash Vasudevan.
60P established a subsidiary, 60P Australia, Pty. Ltd. 60P Australia will take the lead in continuing the company’s development of dengue therapeutics.
Report suggests that the incidence of dengue may have been underestimated by a factor of three. Therefore, prior estimates, including our own, of economic burden and the potential market for dengue drugs, will need to be revised upward.
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60P estimates the potential market for dengue drugs to be $338 million annually. Published in Antiviral Research, the study was based on publicly available information regarding medical costs and lost productivity associated with clinical cases of dengue that result in an estimated economic burden of at least $1.7 billion a year.
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Annual deaths from malaria globally
Travelers to malaria endemic regions per annum
Annual dengue infections globally
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