Kresnier Perez

The Mindact trial, a pivotal study in the realm of breast cancer treatment, has garnered significant attention since its inception. Launched to evaluate the efficacy of genomic testing in guiding treatment decisions for patients with early-stage breast cancer, the trial sought to determine whether such testing could accurately predict which patients would benefit from chemotherapy. […]

Patient recruitment is a critical component of clinical trials, serving as the bridge between the development of new therapies and their eventual availability to the public. The success of a clinical trial hinges on the ability to enroll a sufficient number of participants who meet specific eligibility criteria. This process is not merely a logistical

Health trials, often referred to as clinical trials, are systematic investigations designed to evaluate the safety and efficacy of new medical interventions, including drugs, devices, and treatment protocols. These trials are essential for advancing medical knowledge and improving patient care. They typically follow a structured framework that includes phases—Phase I focuses on safety, Phase II

Health trials, often referred to as clinical trials, are systematic investigations designed to evaluate the safety and efficacy of new medical interventions, including drugs, devices, and treatment protocols. These trials are a cornerstone of medical research, providing the evidence necessary to determine whether a new treatment should be approved for public use. The process typically

Clinical Data Management (CDM) is a critical component of the clinical research process, serving as the backbone for the collection, validation, and analysis of data generated during clinical trials. The primary objective of CDM is to ensure that the data collected is accurate, complete, and reliable, which is essential for making informed decisions about the

The landscape of modern medicine is continually evolving, driven by the relentless pursuit of innovative treatments that can address complex health challenges. Among the most promising avenues of exploration is the therapeutic potential of novel compounds and biological agents that target specific pathways in disease processes. This exploration is not merely an academic exercise; it

The landscape of clinical research has undergone a significant transformation with the advent of technology, particularly in the management of trial documentation. Electronic Trial Master Files (ETMF) have emerged as a pivotal tool in this evolution, replacing traditional paper-based systems with digital solutions that enhance the efficiency and effectiveness of clinical trials. An ETMF is

Real World Evidence (RWE) refers to the clinical evidence derived from the analysis of real-world data (RWD), which encompasses information collected outside of traditional clinical trials. This data can originate from various sources, including electronic health records (EHRs), insurance claims, patient registries, and even patient-reported outcomes. The increasing availability of vast amounts of data has

The Electronic Trial Master File (ETMF) represents a significant evolution in the management of clinical trial documentation. Traditionally, the Trial Master File (TMF) was a physical collection of essential documents that provided evidence of the conduct of a clinical trial and the integrity of the data collected. However, as clinical research has become increasingly complex

Cancer treatment trials, also known as clinical trials, are essential components of the ongoing battle against cancer. These trials are meticulously designed studies that evaluate new treatments, drugs, or procedures to determine their safety and efficacy. They play a pivotal role in advancing medical knowledge and improving patient outcomes. The process of developing a new