Neuroscience

Our team understands the crucial role of rigorous neurological assessments, biomarkers, neuroimaging techniques, and the use of appropriate clinical endpoints in neuroscience trials.

We offer extensive experience across a range of neurological conditions, including:

  • Dementia, Alzheimer's and Parkinson’s Disease
  • Epileptiform disorders
  • Other neurodegenerative diseases
  • Movement disorders
  • Rare genetic neurological conditions

Disciplined,

Cost-Efficient Execution

while maintaining the Highest Quality

Local Trials,

Global Approvals

Access FDA Regulatory Expertise

Our Clinical Team has over

120

years

of Combined Clinical Trial Experience

Addressing Common Pain Points Associated with Neuroscience Clinical Trials 

Neurological disorders can be rare and recruiting enough eligible participants for a study can be challenging. Moreover, due to the chronic or progressive nature of many conditions, retaining participants for the duration of the trial can be tough.

iNGENū CRO addresses this pain point with Enhanced Recruitment Strategies

iNGENū leverages a global network of research sites and patient advocacy groups, utilising advanced data analytics to target and recruit suitable participants efficiently. Through continuous patient engagement and education, we ensure high retention rates throughout our trials.

Neurological outcomes can be subjective and may require specialized scales or biomarkers. Ensuring consistency and reliability in endpoint measurements across different investigators and sites can be challenging.

iNGENū addresses this pain point with Standardization and Training

We implement standardised protocols for all endpoint assessments and provide intensive training for investigators and site personnel. By employing advanced digital tools, we ensure data consistency and reduce variability across sites.

Some neurological interventions, especially those that are invasive or novel, may carry significant risks. Monitoring for adverse events and ensuring participant safety is paramount.

iNGENū addresses this pain point with Rigorous Safety Protocols

We have established robust safety monitoring systems, with real-time data tracking and quick response mechanisms, ensuring the well-being of participants is prioritized at every stage.

Neurological disorders can manifest in various ways in different patients, making it difficult to group patients and interpret results.

iNGENū addresses this pain point with a Personalised Approach

Recognizing the diverse nature of neurological diseases, we employ stratification techniques and personalised medicine approaches. This helps in grouping patients more effectively and interpreting data in a more nuanced manner.

Many neurological disorders progress slowly, requiring long study durations to observe therapeutic effects or disease progression, which can be resource-intensive.

iNGENū addresses this pain point with Innovative Trial Designs

To counteract the long durations often required in neurological trials, we adopt adaptive trial designs, interim analyses, and predictive modeling. This not only accelerates the trial process but also optimizes the use of resources.

Neuroscience Clinical Trial Resources

iNGENu CRO - Alzheimers Disease Clinical Trials

Alzheimer's Disease

From Diagnosis to Clinical Trial Optimization. Addressing key challenges, pivotal endpoints, and strategies to enhance trial success.

iNGENū CRO - Migraine

Migraine

Understanding the Enigma of a Prevalent Neurological Disorder.

 

iNGENu CRO - Phelan-McDermid Syndrome

Phelan-McDermid Syndrome

Navigating Diagnostic Criteria, Trial Endpoints, and Drug Development Challenges.

iNGENuCRO_MS

Multiple Sclerosis

Understanding MS: Epidemiology, Clinical Implications, and Strategies for Clinical Trial Success.

Parkinsons whitepaper cover

Parkinson's Disease

Explore Diagnostic Criteria, Clinical Trial Challenges, and Therapeutic Innovations.

iNGENū CRO - ALS-1

ALS

Dive into Amyotropic Lateral Sclerosis Diagnosis Criteria, Drug Development, and Clinical Trial Challenges.

The iNGENū CRO Difference

iNGENu - FDA
Local Trials, Global Approvals

We uniquely combine Australian expertise with direct FDA submission capabilities, offering a streamlined path for sponsors to achieve global approval. Our seamless integration allows trial data from Australia to be submitted directly to the FDA via our E-Gateway, eliminating the need for third-party intermediaries.

iNGENu - cost efficient
Disciplined, Cost-Efficient Execution

iNGENū CRO takes a highly strategic and disciplined approach to clinical research, ensuring that every dollar is directed toward generating meaningful outcomes. Our trials are designed with efficiency in mind, eliminating unnecessary costs while maintaining the highest scientific and regulatory standards.

iNGENu - APAC
Australian-Headquartered, Asia-Pacific Reach

We provide sponsors with comprehensive trial capabilities across the Asia-Pacific region, offering a seamless combination of cost-efficiency and high-quality clinical trials. We leverage the region's competitive pricing while maintaining rigorous Australian-based project management and clinical oversight.

"We have been using iNGENū for a Phase 1, first-in-human trial of our investigational drug. We have used iNGENū for: Medical writing, project management, clinical data management and full end-to-end, clinical trial execution and monitoring.

We have been very happy with all aspects of the management of the clinical trial and have been particularly impressed by the out-of-the-box creative solutions to speed up and reduce overheads for our company during this clinical trial."

Giles Moss
Chief Executive Officer

iNGENu testimonial-logos-monotone-1

Ready to discuss your Neuroscience Clinical Trial?