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Solid Biosciences to Present at Upcoming Scientific and Patient Advocacy Conferences

Key Takeaway: CAMBRIDGE, Mass., June 23, 2022 (GLOBE NEWSWIRE) -- Solid Biosciences Inc. (Nasdaq: SLDB), a life sciences company focused on advancing meaningful therapies for Duchenne muscular dystrophy (Duchenne), today announced that the Company will participate in the following upcoming sci
Price reaction · baseline $8.2935 (2022-06-22 close) · hit after-hours · clean, no other SLDB news in the window
day 0 close
+8.5%
day 1
+5.4%
day 3 · peak
+14.6%

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+116%
120-day peak, hindsight
Typical move
7.4%
average across 7 past catalysts
Cash runway
~21 mo
Low dilution risk
Lead asset
carmustine
Phase 3 · Lymphoma

Full Press Release Details

CAMBRIDGE, Mass., June 23, 2022 (GLOBE NEWSWIRE) -- Solid Biosciences Inc. (Nasdaq: SLDB), a life sciences company focused on advancing meaningful therapies for Duchenne muscular dystrophy (Duchenne), today announced that the Company will participate in the following upcoming scientific and patient advocacy conferences:
PPMD 2022 Annual Conference – June 23-26, 2022, Scottsdale, AZ
Carl Morris, Ph.D., Chief Scientific Officer at Solid Biosciences, will participate in the Gene Therapy Approaches to Replace or Restore Dystrophin session on Friday, June 24, at 11:30 a.m. EDT / 8:30 a.m. MST.
Event and registration information is available at:
ICNMD 2022 | 17th International Congress on Neuromuscular Diseases – July 5-9, 2022, Brussels, BE
Perry Shieh, M.D., Ph. D. Professor of Neurology and Pediatrics at the University of California, Los Angeles, and an IGNITE DMD investigator, will participate in the PS03: Selected Abstracts for Oral Presentation session on Thursday, July 7, at 10:30 a.m. ET / 4:30 p.m. CEST.
Event and registration information is available at: https://icnmd.org/registration2022/
About Solid Biosciences
Solid Biosciences is a life sciences company focused on advancing transformative treatments to improve the lives of patients living with Duchenne. Disease-focused and founded by a family directly impacted by Duchenne, our mandate is simple yet comprehensive – work to address the disease at its core by correcting the underlying mutation that causes Duchenne with our lead gene therapy candidate, SGT-001, as well as our recently announced next-generation gene therapy candidate, SGT-003. For more information, please visit www.solidbio.com.
Last updated: Jun 23, 2022