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Telix Pharmaceuticals Gets FDA Approval for Prostate Cancer Screening Agent | Global News Avenue

Telix Pharmaceuticals Gets FDA Approval for Prostate Cancer Screening Agent

Key Points

  • Telix Pharmaceuticals reported that the U.S. Food and Drug Administration approved its agent to direct prostate cancer screening.
  • Gozellix is ​​used for PET scan tests for men with positive prostate cancer lesions and patients with possible disease.
  • The Australian biopharmaceutical company started trading in the U.S. four months ago and shares have increased by more than 20% since then.

Stock of Australia-based Telix Pharmaceuticals (TLX) rose 6% on Friday in the United States Food and Drug Administration (FDA) Agents from biopharmaceutical companies are approved for testing for screening for prostate cancer.

Telix explained that the drug Gozellix is ​​used for prostate emission tomography (PET) prostate-specific membrane antigen (PSMA) scans “Prostate cancer has male-positive lesions that question metastasis and is a positive lesions that question metastasis and is a candidate for candidate initial therapy.” It is also designed for people with suspected recurrence based on elevated serum prostate-specific antigen (PSA) levels.

The company explained that Gozellix has a longer shelf life than the current coagulant-based imaging products on the market, “bringing the accuracy and clinical utility of coagulant-based film imaging to more patients in the United States.”

Telix Precision Medicine CEO Kevin Richardson called the FDA decision a “major victory for patients with prostate cancer.”

Telix Pharmaceutical stock only started our trading in November and has grown by more than 20% since then.

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