Alpha Tau Medical Ltd.

Fundamentals7.0
Price Action6.0
News Sentiment7.0
AI Rating
7.0

Key Drivers

  • High liquidity
  • No revenue
  • Significant burn

AI
AI Summary

7.0

Alpha Tau's Japan approval and U.S. radioactive‑material license meaningfully de‑risk the previous binary clinical gamble by creating near‑term commercialization optionality and a tangible liquidity buffer, but the investment now hinges on converting Japan launch into measurable revenue/post‑market data and delivering on‑time positive U.S. pivotal/PMA outcomes to avoid dilutive financing and a sharp re‑rating.

JapanCommercial
Dilution
PMA‍

Price Chart

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Financial Metrics

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Revenue (TTM)
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Net Income (TTM)
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EPS (Q)
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MCAP

Deep Analysis

Research tool. Not personalized advice.

Fundamental Analysis

7.0

Key Financial Insights:

  • High liquidity
  • No revenue
  • Significant burn

DRTS is solvent with strong liquidity and low leverage (~$73M liquid assets vs $28.6M liabilities) but generated zero FY2025 revenue and heavy cash burn (FY net loss $42.6M, operating cash outflow $26.7M), leaving it balance-sheet-backed yet operationally unprofitable.

BalanceSheet
CashBurn

Price Behavior

6.0
Research tool. Not personalized advice. Technical analysis is for informational purposes only.

Key Price Behavior Insights:

  • Below last month average
  • Strong support zone
  • Elevated volatility

Price sits slightly below its last month average (7.26) at $7.07, signaling a mild near-term downward bias with elevated short-term volatility (range ≈ $2.01 or ~28%) and key support around $6.41–$6.70 versus resistance at $7.76–$8.42.

WatchMA
BreakSupport
Support Level: $6.41–$6.70
Resistance Level: $7.76–$8.42

Range of roughly $2.01 (~28% of last month average) indicates elevated short-term volatility

Sentiment & News

7.0

Key News Insights:

  • Japan approval
  • U.S. trial expansion
  • Market entry readiness

Alpha Tau Medical secured Japan's Shonin approval for Alpha DaRT in advanced/recurrent head and neck cancer and announced multiple parallel U.S. trials, new indications and investor outreach as it shifts toward commercialization.

RegulatoryWin
Commercialization

The approval and concurrent trial progress materially de-risk commercial launch and should improve visibility and investor interest as revenue pathways in Japan and other indications accelerate