By NewsDesk @infectiousdiseasenews
TP-05 is designed to kill infected ticks attached to the human body before they can transmit the Borrelia bacteria that causes Lyme disease
Late clinical-stage biopharmaceutical company, Tarsus Pharmaceuticals, announced that it has initiated dosing participants in its first clinical trial for TP-05, a novel, oral, non-vaccine therapeutic for the prevention of Lyme disease.
The Phase 1 Callisto trial is a single ascending dose and multiple ascending dose trial to evaluate the safety, tolerability and pharmacokinetics (PK) of TP-05 in healthy volunteers. There are currently no U.S. Food and Drug Administration (FDA)-approved pharmacological prophylactic options for Lyme disease, which is the most common vector-borne disease in the United States, transmitted to humans through the infection of the bacterium Borrelia burgdorferi
TP-05 is an oral systemic formulation of lotilaner, a well-characterized anti-parasitic agent that paralyzes and kills ticks by selectively inhibiting parasite-specific GABA-Cl channels. TP-05 is believed to be the only non-vaccine, drug-based, preventive therapeutic in development that targets the ticks, and potentially prevents disease transmission. It is designed to rapidly provide systemic blood levels of lotilaner and kill infected ticks attached to the human body before they can transmit the Borrelia bacteria that causes Lyme disease.
“Millions of Americans are at high or moderate risk of contracting Lyme disease, which can lead to significant and long-term health problems. There is a great need for a preventive solution that has the potential to kill the tick before it transmits disease,” said Bobak Azamian, M.D., Ph.D., President and Chief Executive Officer of Tarsus. “Initiating the TP-05 Phase 1 Callisto trial is an important step toward potentially offering a fast-onset and long-acting, oral, non-vaccine therapeutic to help protect those who are at risk for this potentially devastating disease.”
The Callisto trial intends to enroll healthy volunteers and evaluate a wide range of doses of TP-05 in the single dose phase. The multiple dose phase is planned to evaluate different doses of TP-05, each dosed periodically, and determined based on the single dose phase data. In addition to safety assessment, the systemic PK profile of TP-05, including blood levels and epidermal levels, will be assessed to provide valuable information to design future clinical studies and help facilitate exploratory research. The results of this Phase 1 trial are also expected to inform future work on TP-05 for malaria prevention.
“We are evaluating a broad range of doses in this trial to identify the optimal dose to progress to the next phase of research as quickly as possible,” said Sesha Neervannan, Ph.D., Chief Operating Officer of Tarsus. “Advancing TP-05, our second investigational product, to the clinical phase of development is a significant milestone for Tarsus and represents our commitment to address high unmet needs by applying proven science and new technology to revolutionize treatment for patients.”
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