Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
925.00K | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
-17.54M | -3.26M | -3.20M | -2.28M | -1.82M | -340.00K | EBIT |
-97.61M | -55.58M | -56.52M | -50.53M | -41.55M | -24.44M | EBITDA |
-71.44M | -52.29M | -51.99M | -49.59M | -31.46M | -69.10M | Net Income Common Stockholders |
-71.13M | -36.32M | -55.19M | -50.52M | -33.28M | -69.44M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
142.47M | 197.16M | 82.02M | 70.54M | 192.56M | 143.09M | Total Assets |
163.26M | 222.57M | 109.27M | 101.49M | 210.52M | 147.02M | Total Debt |
12.98M | 16.25M | 4.69M | 5.21M | 12.12M | 1.21M | Net Debt |
-129.48M | -131.96M | -77.33M | -65.33M | -180.43M | -141.88M | Total Liabilities |
20.40M | 36.55M | 255.00M | 193.36M | 19.30M | 5.34M | Stockholders Equity |
142.86M | 186.02M | -145.74M | -91.88M | 191.22M | 141.69M |
Cash Flow | Free Cash Flow | ||||
-83.08M | -51.74M | -55.05M | -64.77M | -26.79M | -16.27M | Operating Cash Flow |
-82.62M | -51.42M | -52.82M | -46.40M | -24.57M | -15.39M | Investing Cash Flow |
-5.96M | 25.64M | -2.23M | -18.37M | -2.22M | -688.00K | Financing Cash Flow |
86.01M | 92.48M | 66.53M | 51.06M | 77.14M | 82.24M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
61 Neutral | $2.73B | ― | -31.68% | ― | 32.29% | 64.39% | |
54 Neutral | $3.55B | ― | -214.50% | ― | 29.01% | 23.93% | |
49 Neutral | $6.90B | 0.02 | -54.05% | 2.46% | 24.91% | -3.14% | |
46 Neutral | $3.63B | ― | -19.20% | ― | -89.95% | -123.71% | |
45 Neutral | $675.96M | ― | -238.46% | ― | 71.17% | 23.89% | |
42 Neutral | $38.57M | ― | -270.20% | ― | 144.50% | -141.91% | |
34 Underperform | $370.71M | ― | -66.90% | ― | ― | -342.14% |
Neurogene has updated its corporate presentation, highlighting the progress and future plans for its NGN-401 program for Rett syndrome, which is currently in Phase 1/2 clinical trials. The company is leveraging its proprietary EXACT technology and in-house manufacturing to advance its pipeline and explore market opportunities, positioning itself strategically in the biopharmaceutical sector.
Neurogene’s Phase 1/2 clinical trial for Rett syndrome faced a setback as a participant died from complications linked to a high dose of adeno-associated virus (AAV). The FDA has approved continuing the trial with a reduced dose, influencing future trial designs. This development is crucial for stakeholders monitoring advancements in gene therapy trials.
Neurogene Inc. updates its clinical trial for NGN-401 gene therapy targeting Rett syndrome after a serious adverse event in a high-dose participant led to critical conditions. While the FDA allows continuation at a lower dose, further high-dose enrollments are paused. Safety remains a priority as the trial progresses with no other adverse events reported at lower doses, showcasing potential for future treatments of neurological diseases.
Neurogene Inc. has reported promising interim results from its Phase 1/2 trial of NGN-401 gene therapy for Rett syndrome, highlighting improvements in key areas like motor skills and communication among the first four low-dose pediatric participants. The therapy, which has shown a favorable safety profile, marks significant progress as it addresses the core symptoms of this challenging neurodevelopmental disorder. The company plans to continue the trial with an adolescent/adult cohort and anticipates further updates in 2025, potentially paving the way for a commercial launch.
Neurogene Inc. has announced a $200 million private placement financing, involving top-tier healthcare funds, to support its innovative genetic therapies for rare neurological diseases. The proceeds are expected to fund the company into the second half of 2027, aiding in the development of its NGN-401 gene therapy for Rett syndrome and other projects. Neurogene aims to maximize the therapeutic impact with its EXACT™ platform, ensuring optimized efficacy and safety in its treatments.