Loading...
Market
How many international regulatory approvals will SYMVESS receive by end of 2025?
2
Resolution / Starting Odds
No international approvals • 25%
1 to 2 international approvals • 25%
3 to 4 international approvals • 25%
5 or more international approvals • 25%
Regulatory announcements from international health agencies such as the European Medicines Agency (EMA) or Japan's PMDA
Story
Humacyte Receives FDA Approval for First-in-Class SYMVESS for Treatment of Extremity Vascular Trauma, Stock Surges 61%
Dec 20, 2024, 01:45 PM
Humacyte has received FDA approval for SYMVESS™, the first acellular tissue engineered vessel designed for the treatment of extremity vascular trauma. This innovative product serves as a bioengineered alternative to autologous vein grafts, aimed at improving outcomes in cases of limb-threatening vascular injuries where urgent revascularization is necessary and traditional grafts are not viable. The FDA's approval signifies a notable advancement in medical technology for patients requiring immediate vascular intervention. Following the announcement, Humacyte's stock price surged by approximately 61%, reflecting investor optimism about the product's potential impact in the medical field.
View original story
Similar markets
1-3 countries • 25%
4-6 countries • 25%
7-9 countries • 25%
10 or more countries • 25%
No new competitors • 25%
1 new competitor • 25%
2 new competitors • 25%
3 or more new competitors • 25%
Less than 10% • 25%
10% to 20% • 25%
20% to 30% • 25%
More than 30% • 25%
0-5 • 25%
6-10 • 25%
11-20 • 25%
21+ • 25%
Less than 10 • 25%
10 to 20 • 25%
21 to 30 • 25%
More than 30 • 25%
Less than 5 countries • 25%
5 to 10 countries • 25%
11 to 20 countries • 25%
More than 20 countries • 25%
0-5 countries • 25%
6-10 countries • 25%
11-15 countries • 25%
More than 15 countries • 25%
1-5 countries • 25%
6-10 countries • 25%
11-15 countries • 25%
16+ countries • 25%
0-10 • 25%
11-30 • 25%
31-60 • 25%
61+ • 25%
Less than 10 • 25%
10 to 20 • 25%
21 to 30 • 25%
More than 30 • 25%