Revolution Medicines, Inc. (NASDAQ: RVMDW - Get Free Report) was the recipient of a large increase in short interest during the month of February. As of February 27th, there was short interest totaling 1,369 shares, an increase of 138.9% from the February 12th total of 573 shares. Based on an average daily trading volume, of 11,580
| Name | Quantity | Cost | Value | Profit ($) | Gain (%) |
|---|---|---|---|---|---|
Farallon Capital Farallon Capital Management LLC | 13.72M | $24.39M | $85.92M | $61.53M | 252.23% |
John H. Burbank III Passport Capital LLC | 9.56M | $17.1M | $59.82M | $42.71M | 249.72% |
| AS Alexandra Stickelman Root Financial Partners, LLC | 212 | $115.62 | $1,327.12 | $1,211.5 | 1,047.8% |
| CH Courtney Holt Compound Planning, Inc. | 2,313 | $4,140.27 | $14,479.38 | $10,339.11 | 249.72% |
| TM Tony Macafee UniSuper Management Pty Ltd | 2,800 | $5,012 | $17,528 | $12,516 | 249.72% |
| Biotechnology Industry | Healthcare Sector | Mark A. Goldsmith CEO | NASDAQ (NGS) Exchange | 76155X100 CUSIP |
| US Country | 616 Employees | - Last Dividend | - Last Split | - IPO Date |
Revolution Medicines, Inc. is a clinical-stage precision oncology company dedicated to developing innovative targeted therapies for RAS-addicted cancers. These cancers are notoriously difficult to treat due to mutations in the RAS genes, which are among the most common in cancer. Established in 2014 and based in Redwood City, California, Revolution Medicines focuses on creating RAS(ON) inhibitors and companion inhibitors. These therapies are being designed for monotherapy use, in combination with other RAS(ON) inhibitors, and/or in combination with therapeutic agents, aiming to offer new hope for patients with few existing treatment options.
Revolution Medicines is pioneering the charge against RAS-addicted cancers with its line of RAS(ON) inhibitors. These include:
To complement its RAS(ON) inhibitors, Revolution Medicines is developing RAS companion inhibitors, which are designed for combination treatment strategies to enhance the efficacy of its primary inhibitors. Among them are: