Areas of expertise

Oncology

Oncology clinical trials require a committed team with professional experience in every aspect, facet, and stage of cancer. From radiation oncologists, to surgeons and investigators, experts on cancer research can ensure the successful progression of each clinical trial.

At Clinixir, we guide and support you through your oncological clinical trials with biostatistical analysis. In addition, our experts in their respective fields can develop the right protocols and support for your trials. We provide you with all-encompassing clinical project management services so that your oncology trials meet their timelines and objectives without failure.

We are a reliable one-stop service provider for your clinical research needs. Whether it’s providing you with a complete team to handle all matters related to project management, medical writing, regulatory affairs, site management, or clinical monitoring for a wide range of cancer types, you can be sure to receive our full attention for your oncological trials.
We are also partnered with 8 of Thailand’s leading medical institutions who provide us with additional expert input from top clinical research professionals, further ensuring that your study designs and protocols are ideally structured and meet every regulatory requirement prior to trial commencement. By drawing from this wide range of preclinical experience in oncology, we can deliver fast-track development so that you can conduct your patient studies as soon as possible.

Infectious Diseases

Tackling this global health challenge requires rigorous data collection as well as comprehensive research on the development of new health interventions such as medicines and vaccines. Successful infectious disease clinical trials therefore require experience in managing the myriad complex and urgent challenges that may occur. 

At Clinixir, our expertise in this domain lets us design and deliver timely infectious disease clinical trials in accordance with your requirements. For instance, we are well-prepared to keep your infectious disease clinical trials on the right track throughout each stage of treatment development with time and cost efficient solutions to suit your needs. In addition, our bioanalytical methods for biosafety testing and pharmacokinetic/pharmacodynamic evaluations will help with the determination of your infectious disease drugs, comparators, and validation of new bioanalytical methods. 

Rare Diseases

According to the U.S. Department of Health & Human Services, there are more than 7,000 known rare diseases which continue to impact today’s world. The majority of these diseases have no effective treatments, and most doctors are unable to provide proper diagnosis or treatment plans for the patients involved.

Given the elusive nature of rare diseases, issues related to patient enrollment, unpredictability, retention, and site selection may initially present themselves as challenges. Clinixir’s affiliation with Thailand’s top medical research institutions, and access to the country’s largest set of medical records, can help tackle these problems by keeping you up-to-date with the latest insights on rare diseases and conditions, ensuring that your study designs and protocols are practical, feasible, and realistic.

We prioritize patient enrollment and retention, providing innovative insights aimed at refining the research process. We also offer effective project management, site selection, and advanced solutions for your clinical trials at every stage of development. Furthermore, Clinixir’s researchers have the experience required to help navigate any complexities that may occur during trials. This ensures that your clinical trials are resilient to the different challenges posed by rare diseases, while also producing reliable and actionable data.

We offer expertise on the following rare diseases:

• Tinnitus
• Cystic Fibrosis
• Usher’s Syndrome
• Respiratory Syncytial Virus
• Renal Vasculitis 
• Paroxysmal Nocturnal Dyspnoea 
• Gastroparesis
• Cushing’s Syndrome
• Atypical Hemolytic 
• Acromegaly
• Adrenocortical Carcinoma
• Fibrodysplasia Ossificans Progressiva
• Glomerulonephritis
• Growth Hormone Deficiency
• Lysosomal Storage Diseases
• TTR Amyloidosis 
• Familial Hypercholesterolemia
• Eosinophilic Esophagitis
• Duchenne Muscular Dystrophy

Neurology

Clinical research on neurological disorders requires highly intricate expertise. 

To develop feasible study designs and conduct successful neurological clinical trials, the use of sophisticated technology is necessary. Tools such as magnetic resonance imaging, magnetoencephalography, and electroencephalography are required to monitor, measure, and conduct accurate diagnostic assessments. In addition, a highly experienced and multidisciplinary team is required to identify and track the multitude of ways in which neurological conditions may affect patients.

Clinixir’s research teams possess in-depth knowledge on a wide range of neurological disorders. We can design clinical trials on new neurological treatments and drugs with the aid of cutting-edge diagnostics and reliable outcome measurements at every stage of development. 

Moreover, our neurologists will guide you in planning your studies, staff training, and investigator coordination, while carefully monitoring to ensure that your neurology clinical trials are well executed. 

Metabolic Diseases

Lifestyle changes such as diet and exercise are not always enough to treat metabolic syndrome, and the patients may need other forms of medication or treatment. One primary challenge of coping with metabolic diseases is their complexity regarding diverse causes and symptoms. Careful medical research is necessary to obtain information on the effects of a specific medicine or diet on each person, and their risk of liver disease, heart disease, and diabetes.

Clinixir’s experts on metabolic diseases can help design feasible, cost-effective, and efficient studies to ensure that you meet your research objectives and regulatory requirements. Our knowledge and experience with metabolic disease clinical trials will also ensure that your product’s time to market occurs as planned. We achieve these successful outcomes by testing a variety of models in advance, and referring to medical records to support decision-making throughout the development of each new treatment or drug. Our team will also ensure that the designs, conduct, and analyses of your studies meet the highest standards, resulting in high quality-data which adheres to regulatory filing requirements.

We offer expertise in the following areas: 

• Obesity
• Non-alcoholic Steatohepatitis 
• Dyslipidemia
• Hypogonadism
• Growth Disorders
• Diabetes
• Gout

Herbal Medicines

Herbal treatments and medicines are widely used in Southeast Asian countries, including Thailand. According to research by Mahidol University and North West University, the use of herbal medicines in Thailand is commonly associated with chronic diseases. As a result, herbal medicines play a significant role in clinical trials within the country. However, even though herbal medicines often have therapeutic value, they may also cause adverse reactions. Further research can help minimize these unwanted effects, while preserving the beneficial qualities of these medicines.

Our team at Clinixir has extensive experience evaluating the therapeutic benefits of herbal medicines. We offer operational and strategic solutions for every aspect of drug development, to ensure the effectiveness and safety of each new medication. We can also conduct effective clinical trials on new herbal medicines and treatments in a timely, cost-effective, and well-planned manner. No matter how novel your herbal treatments, our team has the experience to design and conduct herbal clinical trials, and deliver the most reliable data for regulatory filings. 

Medical Devices

All clinical investigations carried out in human subjects involve the use of medical devices. These are used in many stages of medical procedures – including diagnosing illness, treating diseases, and monitoring treatments. It is therefore of fundamental importance to investigate and assess the safety and the performance of these devices.

At Clinixir, we ensure that the clinical products used to conduct our medical device trials meet international standards. Our professionals are certified by the International Conference on Harmonization of Good Clinical Practice (ICH-GCP) for Clinical Investigations of Devices, as well as GCP for Clinical Trials with Investigational Drugs and Medical Devices (US FDA Focus).

Others

The clinical research industry is developing at an unprecedented pace, leading to new and innovative treatments which require further research. These include next-generation targeted immunologic intervention, radioligand therapy, robotic surgery, molecular genetic pathology, medical transplants, and more.

These developing areas of research are currently in their infancy, requiring continuous input from stakeholders and experts in numerous fields. Matters of feasibility, practicality, and commercial potential heavily influence issues surrounding planning, protocol design, and consultancy.

At Clinixir, we strive to discover, research, and innovate new drugs and treatment methods to meet the medical developments of today – and of tomorrow. Our team’s expertise, institutional affiliations, and cutting-edge technology let us provide world-class research solutions for clinical trials, pushing the envelope of knowledge beyond the existing scope of modern research.