Mitchell Efros’ Post

Are you struggling with duplicate and professional research subjects? Look no further than Verified Clinical Trials ™ (VCT)! VCT is a cross-sponsor database that covers phase I-IV across multiple therapeutic indications globally. With VCT, you can save time and money while ensuring your clinical trial meets its endpoints. Contact VCT at connect@verifiedclinicaltrials.com to learn more! #duplicatesubjects #verifiedclinicaltrials #placebo

Are you struggling with duplicate and professional research subjects? Look no further than Verified Clinical Trials ™ (VCT)! VCT is a cross-sponsor database that covers phase I-IV across multiple therapeutic indications globally. With VCT, you can save time and money while ensuring your clinical trial meets its endpoints. Contact VCT at connect@verifiedclinicaltrials.com to learn more! #duplicatesubjects #verifiedclinicaltrials #placebo

Are you struggling with duplicate and professional research subjects? Look no further than Verified Clinical Trials ™ (VCT)! VCT is a cross-sponsor database that covers phase I-IV across multiple therapeutic indications globally. With VCT, you can save time and money while ensuring your clinical trial meets its endpoints. Contact VCT at connect@verifiedclinicaltrials.com to learn more! #duplicatesubjects #verifiedclinicaltrials #placebo

Are you struggling with duplicate and professional research subjects? Look no further than Verified Clinical Trials ™ (VCT)! VCT is a cross-sponsor database covering phase I-IV across multiple therapeutic indications globally. With VCT, you can save time and money while ensuring your clinical trial meets its endpoints. Contact VCT at connect@verifiedclinicaltrials.com to learn more! #duplicatesubjects #verifiedclinicaltrials #placeboresponse

🌟 𝟒,𝟎𝟎𝟎 𝐒𝐜𝐫𝐞𝐞𝐧𝐢𝐧𝐠 𝐕𝐢𝐬𝐢𝐭𝐬 𝐢𝐧 𝟐𝟎𝟐𝟒! 🌟 Thus far this year, Clinibase has proudly seen 4,000 participants attend their first screening visits at trial sites—a moment of true impact for clinical trials. 🙌 The journey from identifying participants, pre-screening them, to that first visit isn’t easy. The “value gap” is significant: thorough pre-screening and scheduling bring potential, but value is only realized when participants show up, ready to contribute to advancing research. These first visits are where meaningful progress begins—not just for participants, but for Sponsors, CROs, and sites relying on timely, reliable recruitment. To the 4,000 participants who took that step: thank you for bridging the gap and making a difference. Here’s to creating even more impact together! 💙 #ClinicalTrials #ParticipantRecruitment #ParticipantsNotLeads #Milestones #Clinibase

Join us next week at the 2024 ISPE Annual Meeting in Berlin on August 28th from 8:00 AM – 1:30 PM for a fascinating poster session presented by AbbVie. Dive into the world of "Unlocking Insights: Lessons Learned from the Tokenization of a Psoriasis Trial" By generating unique patient IDs from personal identifying information, tokenization allows for the seamless integration of clinical trial data with real-world data (RWD), enhancing the capture of comorbidities and drug exposure before a trial even begins. In a recent pilot study using ConcertAI’s claims dataset, researchers successfully integrated trial data with RWD through tokenization, providing valuable insights into the baseline characteristics of trial participants. The results showed a high overlap between trial participants and information in open claims, with some discrepancies noted in closed claims. Despite minor discrepancies in baseline comorbidities between the RCT and RWD populations, the integration of data through tokenization has opened up new possibilities for understanding patient profiles and treatment outcomes. These initial findings highlight the potential of tokenization in bridging the gap between clinical trial data and real-world evidence. Read the abstract to learn more: https://hubs.ly/Q02M6b1D0 #Tokenization #HealthcareResearch #DataIntegration #ClinicalTrials #RWD #HIPAACompliant #PatientID #InnovativeResearch #ISPE2024

🖖🏽 We hear a lot about phases in clinical trials. People who aren't working in research or life sciences will even have heard of them from mainstream media - but what are they and how are they distinct from one another? What exactly is the point? Today, we talk about 4 pretty well-defined phases - and even include "Phase 0" which many are not so familiar with. All phases will have participant and patient safety at their core. Here are the main take-homes from each phase: 0️⃣ Exploratory and generally "proof-of-concept" 1️⃣ Strong focus on dose tolerance in smaller cohorts 2️⃣ Strong focus on product efficacy in larger cohorts 3️⃣ Confirmation of outcomes from earlier trials in much larger cohorts 4️⃣ Post-marketing surveillance for longitudinal monitoring of prescription or off-the-shelf items Learn more here: https://buff.ly/4aX21FE #clinicaltrials #nutritionaltrials #humantrials #epro #ecrf #econsent #ctms #decentralisedclinicaltrials #trialflare

A clinical trial's effectiveness is highly dependent on the trial site's competence and resources and the Sponsor's level of support for the participating sites—Discover Minerva's expertise in overcoming clinical trial challenges. Our solutions redefine research excellence. Join us on the path to a healthier future. #MinervaResearchSolutions #regulatoryhurdles #TRIALTRIBULATIONS #crochallenges #TrialMonitoringIssues #qualitycontrolstruggles #MRS

Practice makes perfect! Launching a new clinical trial requires thorough team preparation. One example is the radioactive water (O15-H2O) trial, sponsored by MedTrace Pharma A/S. This trial explores the efficacy of using O15 to help detect clogged blood vessels and improve detection of coronary artery disease. O15 has a very short half-life of only 2-minutes which requires precise team coordination. Using the MedTrace P3 machine, we quickly convert O15 gas into O15 water. https://hubs.la/Q02vkkHx0 To learn more about this trial, visit: https://hubs.la/Q02vkksv0

How would timely and accurate specimen collection benefit your clinical trial? LabConnect can help make that a reality.