Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
24.12M | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
23.63M | -988.00K | -1.03M | 0.00 | 0.00 | 0.00 | EBIT |
-19.92M | -62.07M | -117.66M | -99.15M | -30.30M | -15.99M | EBITDA |
-20.18M | -58.37M | -111.31M | -204.93M | -118.21M | -24.78M | Net Income Common Stockholders |
-21.27M | -59.50M | -116.42M | -205.21M | -120.30M | -24.02M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
49.27M | 118.65M | 164.65M | 268.02M | 156.74M | 49.27M | Total Assets |
54.05M | 125.89M | 177.01M | 291.39M | 166.19M | 54.05M | Total Debt |
127.96K | 465.00K | 437.88K | 124.52K | 139.86K | 127.96K | Net Debt |
-44.70M | -105.54M | -79.93M | -267.90M | -154.59M | -44.70M | Total Liabilities |
97.33M | 24.85M | 16.81M | 18.82M | 323.20M | 97.33M | Stockholders Equity |
-43.27M | 101.04M | -463.76M | 272.57M | -157.01M | -43.27M |
Cash Flow | Free Cash Flow | ||||
-25.26M | -48.22M | -103.55M | -93.03M | -27.95M | -13.25M | Operating Cash Flow |
-24.82M | -47.93M | -99.27M | -85.57M | -25.61M | -13.09M | Investing Cash Flow |
53.18M | 75.16M | -83.44M | ― | 449.15K | ― | Financing Cash Flow |
-161.72K | -246.00K | ― | 206.66M | 140.74M | ― |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
48 Neutral | $6.35B | 1.09 | -48.69% | 2.63% | 17.17% | 1.01% | |
48 Neutral | $32.66M | ― | -58.89% | ― | ― | ― | |
46 Neutral | $82.90M | ― | -273.36% | ― | 194.23% | 45.50% | |
46 Neutral | $2.80B | ― | -19.20% | ― | -89.95% | -123.71% | |
42 Neutral | $77.93M | ― | -54.21% | ― | -78.55% | -0.92% | |
41 Neutral | $312.86M | ― | -55.13% | ― | -86.25% | 36.10% | |
41 Neutral | $713.24M | ― | -54.00% | ― | 59.55% | 3.09% |
On April 1, 2025, Connect Biopharma announced positive feedback from its Type C meeting with the FDA, which has aligned on the company’s plan to initiate parallel Phase 2 trials of rademikibart for patients with moderate-to-severe asthma or COPD experiencing acute exacerbations. These trials, set to begin in the second quarter of 2025, aim to enroll approximately 160 patients each and will evaluate the efficacy of a single 600 mg subcutaneous dose of rademikibart over 28 days. The company expects to report data from these trials in the first half of 2026, potentially impacting the treatment landscape for asthma and COPD by addressing a significant unmet need.