Today’s Science. Tomorrow’s Cancer treatments.
Our growth strategy is driven by the development of our orphan oncology candidates which aim to answer established and unaddressed therapeutic needs in rare or resistant cancers.
Even though some of our compounds could be used in large oncology indications, we focus on products with at least one potential orphan application and long and solid IP protection as these products with high sales potential benefit from favorable pricing and reimbursement policies and accelerated registration pathways.
We seek to transform scientific opportunities into clinical breakthrough treatments through unparalleled translational expertise, developing products up to the stage where they become compelling opportunities for partners. This means moving products from preclinical stage (1 to 2 years from IND) to optimal inflexion points (usually Phase II clinical proof-of-concept). Once this proof of concept is established, we seek to license these products to pharmaceutical partners, who have the capacity to conduct the registration phases and to market them.
Our added value rests on 3 solid assets:
- A leading-edge scientific expertise in early and breakthrough research fields such as DNA-targeting ;
- Translational research capabilities (bringing a product from the preclinical stage to the proof-of-concept in man) ;
- Our ability to both identify potential targets (already 2 successful mergers / acquisitions) in order to feed our pipeline, and to conclude licensing or partnership agreements (already 4 products sold or licensed to partners).
Onxeo’s orphan oncology products are:
Beleodaq® (belinostat): an HDAC inhibitor, already registered and sold in the U.S. in relapsed or refractory peripheral T-cell lymphoma (PTCL). We are also exploring the value of belinostat beyond PTCL, notably in an oral form, to assess its potential use in various combinations for the treatment of others liquid or solid tumors with filing for a phase I expected by the end of 2017.
AsiDNA™: A first-in-class siDNA (signal-interfering DNA) compound which has successfully undergone a proof-of-concept Phase I trial in metastatic melanoma by intratumoral administration. We are now exploring the potential of AsiDNA™ via systemic administration with the goal to file for a phase I study by the end of 2017.
Livatag® (doxorubicin Transdrug™): its ReLive Phase III study in the treatment of primary liver cancer did not meet the primary endpoint. The product however showed an efficacy similar to the active comparative arm and a good tolerability profile. The prospects of the product are currently under strategic review.
Look up the Orphan oncology products portfolio
Legacy products based on the Lauriad® technology, licensed or sold in 2017
While these products illustrate Onxeo’s undeniable development experience and skills, they are no longer at the heart of the Company’s strategy dedicated to the development of innovative drugs in orphan oncology.
Loramyc®/ Oravig®: indicated for the treatment of oropharyngeal candidiasis and Sitavig®/ Labiriad®, indicated for the treatment of recurrent herpes labialis were developed and registered in Europe and the United States. They were sold to Vectans Pharma in July 2017.
Validive® (clonidine Lauriad®): after positive results of Phase II in the treatment and prevention of radio/chemotherapy induced severe oral mucositis in patients suffering from head and neck cancer, the Company licensed Validive® to Monopar Therapeutics in September 2017.