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Alpha Tau Medical (OTCMKTS:ALTXF) has secured $36.9 million in a registered direct offering, marking a pivotal step in its mission to transform cancer treatment with its groundbreaking Alpha DaRT® technology. The financing, led by an affiliate of Oramed Pharmaceuticals (NASDAQ:ORAM), not only bolsters the company's war chest but also deepens a strategic partnership poised to accelerate commercialization. Here's why investors should pay close attention.

The $36.9 million raised on April 28, 2025, comes at a critical juncture for
Tau. The investment from Oramed's affiliate—purchasing 14.1 million shares at $2.612 per share—extends beyond capital. The partnership includes a three-year strategic agreement under which Oramed will provide investor relations support, business guidance, and capital markets expertise. This collaboration positions Alpha Tau to navigate the complexities of clinical trials and regulatory hurdles more effectively.Notably, Oramed CEO Nadav Kidron has joined Alpha Tau's board, signaling a commitment to shared success. This move aligns with Alpha Tau's CEO Uzi Sofer's emphasis on the timing of the investment, which coincides with four parallel U.S. clinical trials, manufacturing scale-up, and trials targeting multiple internal organs.
Alpha DaRT®'s potential is underscored by recent clinical results. In a combination trial with Merck's Keytruda (pembrolizumab) in head and neck squamous cell carcinoma (HNSCC), Alpha DaRT® achieved a 75% systemic objective response rate (ORR) and a 37.5% complete response rate—far exceeding historical benchmarks of 20-30% ORR for standard therapies. These results, if replicated in larger trials, could position Alpha DaRT® as a first-line treatment for hard-to-treat cancers like pancreatic cancer and glioblastoma multiforme (GBM).
The FDA has already granted Investigational Device Exemption (IDE) clearances for multiple trials, including those in pancreatic cancer and GBM. With upcoming U.S. pilot studies and Japan regulatory submissions on the horizon, Alpha Tau is advancing toward pivotal data readouts that could drive valuation.
As of March 31, 2025, Alpha Tau reported $54.8 million in cash, short-term deposits, and restricted deposits. The $36.9 million infusion brings total liquidity to approximately $91.7 million, providing a runway of roughly 10–12 quarters based on its first-quarter 2025 net loss of $8.7 million. However, this assumes no acceleration in spending—a reasonable assumption given its manufacturing expansion and parallel trials.
While the net loss has grown from $5.8 million in Q1 2024, the increased spending reflects strategic investments in R&D and clinical trials. The MDSAP certification for its manufacturing facility further reduces compliance risks, streamlining entry into global markets like Japan.
Investors should monitor three key catalysts over the next 12–18 months:
1. Clinical Data Releases: Results from ongoing trials, particularly the HNSCC combination trial and pancreatic cancer/GBM pilot studies, could validate Alpha DaRT®'s efficacy and safety profile.
2. Japan Regulatory Approval: Securing approval in Japan—a market with high unmet need for oncology therapies—would open a significant revenue stream and bolster credibility.
3. Manufacturing Scale-Up: Progress in expanding production capacity will determine whether Alpha Tau can meet demand if and when Alpha DaRT® gains approvals.
Despite its promise, Alpha Tau faces material risks:
- Regulatory Hurdles: FDA or Japan PMDA rejections could delay commercialization.
- Clinical Enrollment: Delays in recruiting patients for trials could extend timelines and increase costs.
- Funding Needs: While current cash may suffice for 2–3 years, additional capital may be required for late-stage trials or commercial launch.
For investors willing to accept the risks of early-stage biotech, Alpha Tau presents an intriguing opportunity. Its targeted alpha radiation technology addresses a critical gap in oncology—minimizing collateral damage to healthy tissue while eradicating tumors. The partnership with Oramed adds strategic depth, and the clinical results to date are compelling.
The stock's performance since April 28 (see
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