Valuation : Access Pharmaceuticals, Inc.

Market Cap 339M 292M 275M 251M 469M 32.02B 470M 3.24B 1.26B 16.43B 1.27B 1.25B 52.92B P/E 2026 *
-6.21x
P/E 2027 * -31.5x
Enterprise Value 339M 292M 275M 251M 469M 32.02B 470M 3.24B 1.26B 16.43B 1.27B 1.25B 52.92B EV / Sales 2026 *
6.24x
EV / Sales 2027 * 2.85x
Free-Float
79.59%
Yield 2026 *
-
Yield 2027 * -
Manager TitleAgeSince
Chief Executive Officer 50 15/10/2021
Director of Finance/CFO 42 14/03/2022
Chief Tech/Sci/R&D Officer - 20/10/2025
Director TitleAgeSince
Director/Board Member 58 01/03/2006
Director/Board Member 64 25/03/2021
Director/Board Member 63 19/04/2021
Change 5-day change 1-year change 3-year change Capi.($)
-1.38%+4.79%+46.71%+1.13% 84.22B
-0.57%+0.36%-15.55%-35.15% 60.48B
-2.01%+5.94%+502.08%+33.67% 59.43B
-2.03%-9.22%-7.00%+28.39% 50.31B
-4.58%-2.73%+2.93%+157.71% 48.91B
-1.78%+1.17%+57.96%-16.99% 33.17B
-0.16%+2.78%+49.61%+102.01% 25.95B
-0.19%-4.83%-4.30%+191.74% 22.78B
-1.13%-2.45%+65.99%+110.75% 16.73B
Average -1.56%+0.02%+77.60%+63.70% 44.66B
Weighted average by Cap. -1.69%+0.89%+91.65%+43.32%

Financials

2026 *2027 *
Net sales 54.34M 46.76M 43.99M 40.19M 75.18M 5.13B 75.38M 520M 202M 2.63B 204M 200M 8.48B 119M 102M 96.23M 87.91M 164M 11.22B 165M 1.14B 441M 5.76B 446M 437M 18.55B
Net income -54.51M -46.9M -44.13M -40.31M -75.41M -5.15B -75.62M -521M -202M -2.64B -205M -200M -8.51B -9.22M -7.93M -7.46M -6.82M -12.75M -870M -12.79M -88.19M -34.22M -447M -34.62M -33.86M -1.44B
Net Debt - -
Logo Access Pharmaceuticals, Inc.
Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company developing cell and gene therapies for serious diseases. The Company's ZEVASKYN (prademagene zamikeracel) is an autologous cell-based gene therapy for the treatment of wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa. Its fully integrated cell and gene therapy cGMP manufacturing facility in Cleveland, Ohio serves as the manufacturing site for ZEVASKYN commercial production. Its development portfolio features adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with high unmet medical need. Its AAV capsids are being evaluated to improve tropism profiles for a variety of devastating diseases. Its pipeline programs include ABO-504 (Stargardt disease), ABO-503 (X-linked retinoschisis), ABO-505 (autosomal dominant optic atrophy), UX111 (Sanfilippo Syndrome Type A (MPS IIIA)), TSHA-102 (Rett Syndrome), and TSHA-118 (Infantile Batten Disease (CLN1 Disease)).
Employees
-
Trader
Investor
-
Global
-
Quality
-
ESG MSCI
-