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| Date | Price Target | Rating | Analyst |
|---|---|---|---|
| 6/27/2024 | $65.00 | Outperform | BMO Capital Markets |
| 6/11/2024 | $54.00 | Outperform | Robert W. Baird |
| 4/29/2024 | $46.00 | Outperform | Leerink Partners |
| 3/21/2024 | $61.00 | Outperform | William Blair |
4 - Neurogene Inc. (0001404644) (Issuer)
4 - Neurogene Inc. (0001404644) (Issuer)
4 - Neurogene Inc. (0001404644) (Issuer)
BMO Capital Markets initiated coverage of Neurogene with a rating of Outperform and set a new price target of $65.00
Robert W. Baird initiated coverage of Neurogene with a rating of Outperform and set a new price target of $54.00
Leerink Partners initiated coverage of Neurogene with a rating of Outperform and set a new price target of $46.00
BMO Capital analyst Keith Tapper initiates coverage on Neurogene (NASDAQ:NGNE) with a Outperform rating and announces Price Target of $65.
Expanded Phase 1/2 gene therapy trial for Rett syndrome to inform future registrational study design; Company remains on track to share interim clinical data in 4Q:24 Strong financial position with runway into 2H:26 following reverse merger and private financing in December 2023 Neurogene Inc. (NASDAQ:NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced fourth quarter and full year 2023 financial results and highlighted recent corporate updates. "We started the year with strong execution in our Phase 1/2 NGN-401 gene therapy trial for female pediatric patients with Rett syndrom
SC 13G - Neurogene Inc. (0001404644) (Subject)
SC 13G - Neurogene Inc. (0001404644) (Subject)
Financing included participation from top-tier healthcare funds Proceeds expected to fund Company into the second half of 2027 Company to host webcast to review interim clinical data from Phase 1/2 trial of NGN-401 gene therapy for Rett syndrome on November 11 at 4:30 p.m. ET Neurogene Inc. (NASDAQ:NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced that it has entered into a securities purchase agreement for a private investment in public equity ("PIPE") financing that is expected to result in gross proceeds of approximately $200 million to Neurogene, before placement agent fees
Company to host webcast to review data on November 11 at 4:30 p.m. ET Late-breaker poster to be presented during Child Neurology Society Meeting on November 12 Neurogene Inc. (NASDAQ:NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced that it will host a webcast to present interim efficacy data from the low-dose cohort of its ongoing Phase 1/2 clinical trial of NGN-401 gene therapy for pediatric patients with Rett syndrome on November 11, 2024 at 4:30 p.m. ET. Safety data from the low- and high-dose cohorts will also be shared. These data will also be presented in a late-breaking
NGN-401 gene therapy for Rett syndrome received RMAT designation from FDA based on preliminary clinical evidence indicating the potential to address unmet medical needs NGN-401 selected for FDA START Program, also designed to accelerate development Interim NGN-401 efficacy data from Cohort 1 remains on track for 4Q:24 Neurogene Inc. (NASDAQ:NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced second quarter 2024 financial results and highlighted recent corporate updates. "We are pleased that NGN-401 gene therapy for Rett syndrome received RMAT designation, in addition to the
8-K - Neurogene Inc. (0001404644) (Filer)
10-Q - Neurogene Inc. (0001404644) (Filer)
8-K - Neurogene Inc. (0001404644) (Filer)
Company to host webcast to review data on November 11 at 4:30 p.m. ET Late-breaker poster to be presented during Child Neurology Society Meeting on November 12 Neurogene Inc. (NASDAQ:NGNE), a clinical-stage company founded to bring life-changing genetic medicines to patients and families affected by rare neurological diseases, today announced that it will host a webcast to present interim efficacy data from the low-dose cohort of its ongoing Phase 1/2 clinical trial of NGN-401 gene therapy for pediatric patients with Rett syndrome on November 11, 2024 at 4:30 p.m. ET. Safety data from the low- and high-dose cohorts will also be shared. These data will also be presented in a late-breaking