Elanco Animal Health Incorporated (NYSE: ELAN), an American animal health company, announced on Monday that the US Food and Drug Administration has approved label expansions for Elanco's canine parasiticides Credelio Quattro and Credelio.
The updated labels add prevention of Lyme disease as a direct result of killing black-legged ticks (Ixodes scapularis) and treatment and control of longhorned tick (Haemaphysalis longicornis) infestations.
Both products contain the active ingredient lotilaner, which the company says is highly effective at killing black-legged ticks and demonstrated 100% efficacy against longhorned tick at 48 hours in a peer-reviewed study.
The Companion Animal and Parasite Council tracker shows more than 422,000 cases of Lyme disease in dogs in the United States so far this year, surpassing total annual cases seen in 2019.
Elanco emphasised the rising threat from ticks, noting the longhorned tick is rapidly spreading and now present in 22 US states. Company executives have characterised the label expansion as enhanced protection for dogs and a response to this increasing tick-borne disease risk.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval