Compare QRVO & TGTX Stocks: Price Trends, ML Decisions, Charts, Trends, Technical Analysis and more.
Current Price
Current Price
| Metric | QRVO | TGTX |
|---|---|---|
| Founded | 1957 | 1993 |
| Country | United States | United States |
| Employees | N/A | N/A |
| Industry | Semiconductors | Biotechnology: Pharmaceutical Preparations |
| Sector | Technology | Health Care |
| Exchange | Nasdaq | Nasdaq |
| Market Cap | 7.9B | 7.9B |
| IPO Year | 2014 | 2008 |
| Metric | QRVO | TGTX |
|---|---|---|
| Price | $105.29 | $54.65 |
| Analyst Decision | Hold | Strong Buy |
| Analyst Count | 13 | 5 |
| Target Price | ★ $90.64 | $49.80 |
| AVG Volume (30 Days) | 832.8K | ★ 1.8M |
| Earning Date | 05-05-2026 | 05-04-2026 |
| Dividend Yield | N/A | N/A |
| EPS Growth | 524.14 | ★ 1746.67 |
| EPS | ★ 3.62 | 0.17 |
| Revenue | ★ $3,678,517,000.00 | $2,785,000.00 |
| Revenue This Year | $0.81 | $49.08 |
| Revenue Next Year | N/A | $26.69 |
| P/E Ratio | ★ $28.75 | $326.94 |
| Revenue Growth | ★ N/A | N/A |
| 52 Week Low | $75.43 | $26.76 |
| 52 Week High | $109.49 | $59.30 |
| Indicator | QRVO | TGTX |
|---|---|---|
| Relative Strength Index (RSI) | 72.89 | 53.05 |
| Support Level | $92.89 | $51.51 |
| Resistance Level | $109.49 | $58.04 |
| Average True Range (ATR) | 2.75 | 2.79 |
| MACD | 0.79 | 0.16 |
| Stochastic Oscillator | 97.11 | 54.76 |
Qorvo represents the combined entity of RF Micro Devices and TriQuint Semiconductor, which merged in January 2015. The company specializes in radio frequency filters, power amplifiers, and front-end modules used in many of the world's most advanced smartphones. Qorvo also has a suite of products sold into a variety of non-smartphone end markets, such as wireless base stations, cable TV and networking equipment, and infrastructure and military applications.
TG Therapeutics Inc is a fully integrated, commercial-stage biotechnology company focused on acquiring, developing, and commercializing novel treatments for B-cell diseases. In addition to a research pipeline, TG Therapeutics has received approval from the U.S. Food and Drug Administration (FDA) for BRIUMVI (ublituximab-xiiy) to treat adult patients with relapsing forms of multiple sclerosis (RMS), including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, as well as approval from several regulatory agencies outside of the U.S. for BRIUMVI to treat adult patients with RMS who have active disease defined by clinical or imaging features.