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Profound Medical Announces Health Canada Approval of TULSA-PRO®

Key Takeaway: Profound Medical Corp. has received Health Canada approval for its TULSA-PRO® system, designed for the radiation-free ablation of low to intermediate risk organ-confined prostate cancer. This innovative system combines real-time MRI, thermal ultrasound, and closed-loop temperature feedback control, marking a significant advancement in prostate cancer treatment.
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Market Sentiment Analysis

POSITIVE FACTORS

  • Health Canada approved the TULSA-PRO® system.
  • The system offers a customizable, incision-free therapy.
  • It uses advanced technology like MRI and thermal ultrasound.
  • The approval targets low to intermediate risk prostate cancer.

Full Press Release Details

TORONTO, Nov. 25, 2019 (GLOBE NEWSWIRE) — Profound Medical Corp. (NASDAQ:PROF; TSX:PRN) (“Profound” or the “Company”), the only company to provide customizable, incision-free therapies which combine real-time Magnetic Resonance Imaging (“MRI”), thermal ultrasound and closed-loop temperature feedback control for the radiation-free ablation of diseased tissue, today announced Health Canada approval of the TULSA-PRO® system for the ablation of low to intermediate risk organ-confined prostate cancer.

Frequently Asked Questions

What is TULSA-PRO®?

TULSA-PRO® is a system for the radiation-free ablation of prostate cancer.

Who approved the TULSA-PRO® system?

The TULSA-PRO® system was approved by Health Canada.

What technology does TULSA-PRO® use?

It combines real-time MRI, thermal ultrasound, and closed-loop temperature feedback.

What type of cancer does TULSA-PRO® target?

It targets low to intermediate risk organ-confined prostate cancer.

Last updated: Feb 19, 2024