Biopharmaceutical company Lysogene (Paris:LYS) on Friday revealed that its cash and cash equivalents amounted to EUR26.5m as of 31 December 2019.
This marks a decline when compared with cash and cash equivalents of EUR29.1m as of 30 September 2019.
The 2019 cash and cash equivalents include the payments from Sarepta Therapeutics Inc related to the milestone payment and development cost reimbursement triggered by dosage of the first patient in AAVance, the Phase 2/3 clinical trial of LYS-SAF302 in MPS IIIA. The license and collaboration agreement with Sarepta Therapeutics Inc generated in 2019 revenues of EUR12.0m.
At the end of 2019, the cash position is in line with the company's expectations and allows to serenely advance the development programme of the 16th patient under its Phase 2/3 clinical trial of LYS-SAF302 in MPS IIIA, said Karen Aiach, founder and CEO.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA