ImmuPharma PLC (LSE:IMM), (“ImmuPharma” or the “Company”), the specialist drug discovery and development company, is pleased to announce its preliminary audited results for the year ended 31 December 2013.
- Discussions continue with potential partners in parallel to discussions with Contract Research Organisations and alternative financing organisations for LupuzorTM’s pivotal Phase III programme – Special Protocol Assessment (SPA) and Fast Track Designation granted by FDA.
- Granted an amended SPA by the FDA in 2013 reducing the number of patients required to complete Phase III.
- Manufactured drug product for phase III. Plan to file the non-clinical part (except DMF) of the NDA (New Drug Application) to the FDA.
- Established world class Scientific Advisory Board of prominent physicians and advisors in the field of lupus to provide guidance and support for LupuzorTM’s phase III programme.
- Cancer: Phase I/IIa clinical trial ongoing with the next generation “polyplexed Nucant” formulation in three European hospitals including the prestigious Institute Jules Bordet in Belgium.
- New exciting indications discovered:
- Cancer: Development of novel applications of the Nucant family of peptides targeting combination therapies.
- Angiogenesis: age-related macular degeneration, diabetic retinopathy.
- Collaboration established with the University of Bordeaux in coordination with the CNRS to identify and patent novel peptide drugs.
- New technology patented with a target first application in diabetes.
- Signed a £50 million equity finance facility with Darwin Strategic Limited
- Cash position as at 31 December 2013 of £5.4m (2012: £8.9m)
- Loss for the period of £3.7m (2012: £3.8m)
- Basic and diluted loss per share was 4.52p (2012: 4.71p)
- Continued successful relationship with the CNRS, the largest fundamental research institute in Europe