ORTHOPAEDICS
CYCLOLAB - WITH THE USE OF LICENSED SWISS TECHNOLOGY PRESENTS SOLUTIONS FROM DISCOVERY TO COMMERCIALIZATION PHASES, USING A NEW GENERATION OF DRUG SERIES AND DOSAGE FORMS
EFFICACY
The therapeutic efficacy drug series and dosage forms of a new generation has been achieved by combining special formulations in which different cyclodextrins (Dexolve, Q.DIMEB, HPBCD, HPGCD) with API potential are also present.
SAFETY
Possessing targeted, sorption properties with detoxicant effects, hypoallergic nature, and a number of other innovative solutions in a single formulation - demonstrating not only absolute drug safety, but also a wide range of complex therapy in synergy with TOP drugs distributed on the market.
ANALYTICS
Cyclolab provides the potential partner with evidence-based analysis of pre-clinical, clinical and post-clinical studies in a personalized manner prior to entering into a contractual relationship, offering seamless exclusivity of the technology transfer phase.

TURNKEY SOLUTIONS - FROM THE DISCOVERY PHASE TO THE TECHNOLOGY TRANSFER

Personalized services: formulations - Exclusive drugs tailored right in the palm of our Partners hands.

Turnkey Solutions - from the Discovery Phase to the Technology Transfer
Ever since 1973 our team has been specializing in the development of a new generation of APIs through scientific research programs in the discovery phase, preclinical- and clinical studies, as well as technology transfer.

  • Our pharmaceutical formulations are aimed to ensure restoration of physiological processes in cells, organs, and bodily functions due to their uniquely combined* properties of each individual formulation, and in variations of the drug administration routes.
  • *The combined pharmaceutical compositions are characterized by the presence of API variations released for the first time into the world market. This includes our unique excipient ingredients, which also reveal the synergistic potential of our API properties.
Exclusive new-generation pharmaceutical active ingredients and excipients are demonstrated in ready-to-use, effective and safe formulations, which are characterized by non-analogous benefits for modern medicine:

THE MECHANISM OF ACTION OF THE THERAPY

For the first time in the world - drug formulations - therapeutic donors/convectors of synthesis of singlet oxygen (ROS) in the body.

The development of irreversible pathologies in the human body requires a significant amount of oxygen (the enzyme NADP-H is an immune reaction of phagocytes), as well as a stock of available oxygen for ROS synthesis.

To mobilise the required dissolved O2 and activate ROS synthesis, an oxygen donor must be applied. Oxygen adsorbed on the surface of the compositions of the formulation ingredients is a suitable therapeutic donor source. NADPH-oxidase (NOX) is one of the major sources of cellular reactive oxygen species (ROS) and is formed by catalysis.

Role of ROS - targeting reaches the site of infectious infiammation and interacts with NADP-H of immune cells of phagocytes and macrophages, causing numerous cytomorphological changes in them, thereby triggering apoptotic or necrotic type of pathogenic cell death.

ROS synthesis - toxic to cellular pathogens, destroys pathogenic agents and molecules. At the same time, healthy cells are not damaged because, unlike virus-infected cells, healthy cells have antioxidant enzyme systems.

ROS synthesis in the body - targeting, therapeutic ideal safety, is due to the localisation of the infiammatory process induced, provoked by macrophages in response to pathogens of viral etiology (SARS Cov-2 and their subsequent mutations).

Target penetration into problematic cells of the organism, reaching the site of infiammation of infectious nature is due to the immune reaction, i.e. increase (multiple of 10÷15 times) of oxygen demand in the foci of infiammation on the enzyme complex NADPH-oxidase.

Which catalyses the formation of superoxide free radical by transferring one electron to oxygen from NADPH, playing an important role in immunity, cell signalling (NADPH + 2O2 <--> NADP+ + 2O2- + H+)

In the electron transport chain, during the reaction of oxygen with reducing compounds NADH, the redox energy stimulates the synthesis of adenosine triphosphate (ATP), which is the main source of energy for living cells.

SYNOPSIS OF THE COOPERATION STEPS TOWARDS OUR LONG-TERM MUTUALLY BENEFITIAL CO-OPERATION

To know more about the selected nosology(-ies), we recommend that you visit the Application Form section, where you can learn more about nosologies, disease groups and subgroups. You will also learn about CTA files and technology transfer, routes of drug administration, registration statuses, and other aspects of the service by filling in the sections of interest in an interactive form. Once you have completed the relevant sections, you will receive personalized offers and files with detailed information on the readiness of the technology. The aim is for the Applicant’s company to make a decision proceeding to Step 1 - 'Registration'.

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• Please note that the submitted version of your Application Form is final. Our partners dynamically declare the indication of exclusivity in market territories and routes of drug administration. Due to this and other factors, we recommend you to indicate your initial wishes and strategic ones (such as license reservation in the diseases of interest) in order to reserve your priorities.