Earnings Call Summary | MediWound(MDWD.US) Q4 2023 Earnings Conference
Earnings Call Summary | MediWound(MDWD.US) Q4 2023 Earnings Conference
The following is a summary of the MediWound Ltd. (MDWD) Q4 2023 Earnings Call Transcript:
以下是MediWound Ltd.(MDWD)2023年第四季度财报电话会议记录摘要:
Financial Performance:
财务业绩:
MediWound reported full year 2023 revenue of $19 million, driven largely by sales of NexoBrid in the U.S., Japan, and India.
Projection for the fiscal year 2024 is estimated around $24 million and the revenues are expected to hit $39 million in 2026.
The Q1 2023 revenue was $5.3 million, a decrease from Q1 2022's $11.6 million in revenue. The primary reason was the absence of the BLA approval milestone payment from Vericel.
The company triggered an operating loss of $3.9 million in Q1 2023, compared to an operating profit of $2.1 million in Q1 2022.
Net loss for Q1 2023 was $1.7 million or $0.19 per share, a decrease from a net loss of $7.5 million in Q1 2022 due to a favorable adjustment from the revaluation of warrants.
MediWound报告称,2023年全年收入为1900万美元,这主要是由NexoBrid在美国、日本和印度的销售推动的。
预计2024财年约为2400万美元,收入预计将在2026年达到3,900万美元。
2023年第一季度的收入为530万美元,较2022年第一季度的1160万美元收入有所下降。主要原因是Vericel没有按照BLA的批准里程碑付款。
该公司在2023年第一季度引发了390万美元的营业亏损,而2022年第一季度的营业利润为210万美元。
由于认股权证重估进行了有利的调整,2023年第一季度的净亏损为170万美元,合每股亏损0.19美元,低于2022年第一季度的750万美元净亏损。
Business Progress:
业务进展:
A Phase III trial for EscharEx is imminent. This product targets a $2 billion market and has shown superior performance over the current market leader in Phase II studies.
MediWound gained approval for NexoBrid for pediatric use in Europe and is under FDA review for similar approval in the U.S.
Expanded manufacturing facilities due to a surge in demand for NexoBrid. The expansion is scheduled to complete by mid-2024.
Research collaborations have been initiated with 3M, Mölnlycke, and MIMEDX for the upcoming EscharEx Phase III study.
The company secured a total of $23 million in R&D funding from the U.S. Department of Defense and from BARDA for the ongoing development of NexoBrid.
A project funded by DoD at $13 million is underway to transition the product to room temperature storage, which would simplify supply chains and administration.
Upcoming meetings with the FDA to discuss the development path and potential commercial activities under a license agreement with Vericel.
eSchareX的三期试验迫在眉睫。该产品的目标市场规模为20亿美元,在II期研究中,其表现优于目前的市场领导者。
MediWound获得了欧洲儿科用途的批准,并正在接受美国食品药品管理局的审查,以获得类似的批准。
由于对NexoBRID的需求激增,制造设施有所扩大。扩建计划于2024年中期完成。
已经开始与3M、Monlycke和MIMEDX就即将到来的Escharex III期研究进行研究合作。
该公司从美国国防部和BARDA获得了总计2300万美元的研发资金,用于NexoBrid的持续开发。
一个由国防部资助的1300万美元项目正在进行中,该项目旨在将该产品过渡到室温存储,这将简化供应链和管理。
即将与美国食品药品管理局举行会议,讨论与Vericel签订的许可协议下的开发路径和潜在的商业活动。
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