Clinical Trials

  • Clinical Trials
  • Altasciences Appoints New General Manager, Clinical Operations

    Laval, Québec, Monday, January 29, 2024Altasciences announced the appointment of James Brazeal as General Manager, Clinical Operations, at its clinical facility in Kansas City.

    James joined Altasciences, having previously worked as Vice President of Research at Akron Children’s Hospital, and most recently as Vice President of Research Operations for Circuit Clinical. 

    “James’ proven leadership skills, and deep knowledge of all phases of clinical research, will be invaluable in delivering expert guidance for our clients along their early-phase clinical journey,” said Ingrid Holmes, Vice President, Clinical Operations, Altasciences.

    With close to a decade of experience in the healthcare and pharmaceutical sectors, including clinical pharmacology, James will apply his knowledge to oversee the day-to-day management of clinical operations at Altasciences’ 140-bed, Phase I clinical pharmacology unit in Kansas City.

    “It is rewarding to be joining a team that has been in place for almost three decades, a team committed to quality, excellence, integrity, and respect—focused on helping to bring better therapies to the patients who need them, faster,” says James. 

     

    About Altasciences

    Altasciences is an integrated drug development solution company offering pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing, and analytical services. For over 25 years, Altasciences has been partnering with sponsors to help support educated, faster, and more complete early drug development decisions. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology and proof of concept, bioanalysis, program management, medical writing, biostatistics, clinical monitoring, and data management, all customizable to specific sponsor requirements. Altasciences helps sponsors get better drugs to the people who need them, faster. To learn more about Altasciences, visit altasciences.com.
     

    Julie-Ann Cabana
    Altasciences
    +1 514 601-9763
    jcabana@altasciences.com  

    Regulatory Comparisons for Starting First-In-Human Clinical Trials

    A Closer Look At Our On-Site Compounding Pharmacies

    Altasciences' dedicated pharmacists bring a wealth of expertise in controlled substances and complex compounding, ensuring maximum precision and safety standards.

    What you can expect:

    Cutting-Edge Facilities

    - USP 797 certified clean rooms with Class II biological safety cabinets.
    - Negative pressure, HEPA-filtered extemporaneous compounding rooms equipped with the advanced PowderSafe™ ductless balance enclosure, guaranteeing sterile and controlled environments for multiple dosage forms.
    - Electronic security access to the pharmacy and video monitoring.
    - 24/7 monitoring of temperature and humidity.


    Regulatory Excellence
    - Licenses for Schedule I through IV drug substances.
    - Adherence to harmonized pharmacy-specific SOPs based on cGMP principles at our      three clinical pharmacology units.
    - Exceptional inspection results from major regulators such as the FDA, HC, EMA, and MHRA.


    Comprehensive Capabilities 
    - Extensive experience in extemporaneous and intravenous preparation, including biologics.
    - Fully equipped to support all types of IP administration forms.


    Clinical Supply Manufacturing
    Integration with our manufacturing team, ensuring flexibility and adaptability to meet the evolving needs of your studies throughout your drug development program or study.

    BOOK A VISIT

     

    You may also be interested in the following webpages:​​​

    Clinical Research Services

    Pharmaceutical CDMO and Contract Manufacturing Services


    DID YOU KNOW?
    Our CDMO team offers formulation development and manufacturing of your API, from discovery through commercialization. We also provide analytical testing, ICH stability storage and testing, as well as finished product and release testing. We can manufacture almost every dosage form on the market.

    Start Your Clinical Trials Faster... 70% Faster!

    The Secret to Accelerated
    Drug Development


    Our latest case study showcases how we started a Phase I study in just 3.5 weeks, 70% quicker than the industry’s 12-week standard. 

    The secret to our success? Effective communication, strategic planning, optimal delegation of responsibilities, and removal of silos.

    We aligned our internal team on all objectives, engaged in open dialogue with the sponsor throughout the study, and optimized project management by assigning two leads in two different time zones—expediting decision-making. This case study is your roadmap to faster drug development. 

    READ FULL CASE STUDY


    Contact us to discuss how we can accelerate your study start-up timelines.

    Think Ethnobridging Sooner!

    Planning a Phase I clinical trial? Consider an ethnobridging strategy.
     

    By conducting vital analyses on Asian participants during Phase I studies conducted in Western regions, you can significantly cut costs and shorten the NDA timeline. This strategy streamlines the approval process in Asian markets and addresses potential disparities in drug metabolism between Asian and non-Asian populations.

    Here are some key resources for ethnobridging in Phase I clinical trials:

    In this issue of The Altascientist, we demonstrate how ethnobridging can prevent the need for region-specific development programs, helping you safely achieve commercial milestones more efficiently.

    DOWNLOAD YOUR COPY TODAY

     

    In this complimentary webinar, Mel B. Affrime, PharmD, Executive Vice President, Translational Medicine, discusses how ethnic differences can impact the bioavailability of your drug candidate and how to design a multiregional clinical development program to hasten worldwide regulatory approval safely.

    WATCH THE WEBINAR

     

     Speak with an expert today to discuss your next clinical program.

    You may also be interested in the following webpages:​​​

    Ethnobridging Clinical Trials
    Early Clinical Development Services — Phase I/II


    Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.


    Say Goodbye to Clinical Trial Delays!

     

    Your Passport to Success 

    At Altasciences, we understand the importance of streamlining your drug development process and ensuring the highest quality results. We provide a comprehensive, North American solution that significantly enhances the clinical trial phase, from design and conduct to compiling data for regulatory submission.

    Here's why Altasciences is your ideal CRO partner:

    1. We conduct trials in both Canada and the U.S.
      You can experience expedited timelines by conducting trials in Canada, giving you a competitive edge right from the start. Our expertise in navigating Health Canada's CTA process ensures smooth and efficient approvals. Discover more: An Overview of Health Canada's CTA Process
       
    2. We have optimized workflows for efficient bioanalytical sample processing.
      Save time with our optimized workflows that ensure timely processing, transport, and analysis of your samples. Our co-located clinics and labs in both Canada and the U.S. work seamlessly to accelerate your data. Watch how: Accelerate Your Data With Our Canadian Co-located Clinic and Lab
       
    3. We can prevent repeated Phase I studies for drugs intended for the Asian market.
      Speed up approval of your drug in Asian markets by conducting your trials at our clinical site in L.A., one of the most ethnically diverse regions in the U.S. Our expertise in ethnobridging trials can pave the way for your global market access. Learn more: Shortening Drug Development Timelines With Asian Ethnobridging Trials
       
    4. We have driving simulators on-site.
      For CNS drugs that need assessment of their impact on driving ability, start your study faster and with lower costs thanks to our on-site driving simulators in Montréal. 13,000+ simulated drives completed to date! Learn how: Studying the Effects of Drugs on Driving
       
    5. We specialize in human abuse potential assessments.
      Benefit from experience at our Kansas City clinical site—we have successfully conducted over 60 HAP studies, including for stimulants, opioids, and sedative-hypnotics. Read more: Assessing Human Abuse Potential to Limit the Misuse and Abuse of Prescription Drugs
       
    6. We offer specialized ophthalmology expertise.
      Benefit from combined clinical and scientific expertise specific to ophthalmology and our co-located ophthalmic clinic. See how: Co-located Canadian Ophthalmology Center for All Your Early Phase Development Needs

       

    Schedule a chat with our experts to learn more about how Altasciences can be your only North American clinical trial solution. Contact Us to get started.

     

    [Video] Watch and Smile – Our Canadian Team in Action

     

    Think Canada!

    If you have yet to visit our Montréal clinical facility to learn about the advantages of conducting trials in Canada or had the pleasure of meeting the friendly, uniquely talented, and experienced team working on your studies, you will want to watch our latest video

    Think Montreal


    You may also be interested in the following:

    •    Webpage: Clinical Research Services
    •    Scientific Journal: The Advantages of Conducting Early Phase Clinical Research in Canada
    •    eBook: Altasciences' Facilities: Moving in Unison

     

     

    September is pain awareness month, and the importance of pain management and continued research into effective analgesics is integral to helping patients suffering from various pain conditions.

    Altasciences' Facilities: Moving in Unison

    Altasciences Completes Successful Phase I Trial of Ischemix’ Novel Compound for Treatment of Traumatic Brain Injury (TBI)

    Laval, Québec, August 30, 2023Altasciences is pleased to have completed a Phase I trial on Ischemix, Inc.’s novel, proprietary cytoprotective drug candidate, CMX-2043, for the treatment of acute TBI. The trial was performed at Altasciences’ clinical facility in Montréal. 

    The Phase I trial was performed to evaluate safety, tolerability, and pharmacokinetics in a group of 80 healthy participants in a two-part, double-blind, placebo-controlled study. Single ascending doses (SAD) of CMX-2043 were administered by brief intravenous infusion to 40 male and female participants. Once completed, an additional 40 male and female participants were randomized and received multiple ascending doses (MAD) in the same manner, over five days. The results of the trial showed a well-characterized pharmacokinetic profile, demonstrating dose proportionality over the ranges studied.

    “This Phase I trial demonstrates that CMX-2043 has the potential for an excellent safety profile when given intravenously over a wide range of doses”, explained Jerry O. Stern, MD, Chief Medical Officer for Ischemix. “There were no serious adverse events, and all treatment-emergent adverse events were mild and self-limiting. Importantly, the Principal Investigator determined that few adverse events were drug-related.”

    There are no TBI-specific therapies approved for the treatment of patients suffering brain injury, yet it is estimated that in the U.S. TBI is responsible for 60,000 deaths per year, and the cause of 80,000 cases of permanent disability.

    “It was a pleasure collaborating as the Principal Investigator on this clinical study. We are extremely pleased with the outcome of the CMX-2043 Phase I trial. Having personally witnessed first-hand the outcome that TBI can have on the lives of many people, we hope that the work we are doing with Ischemix will continue to progress. If successful, this treatment could have a tremendous positive impact on the quality of life for TBI patients. That is incredibly rewarding,” stated Dr. Morelli, MD, Chief Medical Officer and Principal Investigator for Altasciences. “We wish the team at Ischemix continued success on the next Phase of clinical research.”

    Additionally, Co-chief Operating Officer, Marie-Hélène Raigneau, said of the study: “Our goal at Altasciences is to help companies like Ischemix expedite the drug development process without compromising on quality or safety. We are proud to support Ischemix in advancing this vital new therapy.”

    Ischemix expects to complete all of the work required for a Phase II trial of CMX-2043 in acute TBI by the end of 2023, and plans to request a pre-IND meeting with FDA for early Q1 2024.


    About Altasciences
    Altasciences is an integrated drug development solution company offering pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing, and analytical services. For over 25 years, Altasciences has been partnering with sponsors to help support educated, faster, and more complete early drug development decisions. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology and proof of concept, bioanalysis, program management, medical writing, biostatistics, clinical monitoring, and data management, all customizable to specific sponsor requirements. Altasciences helps sponsors get better drugs to the people who need them, faster. To learn more about Altasciences, visit altasciences.com


    About Ischemix, Inc.
    Ischemix Inc. is a privately held drug development company based in Grafton, MA. Learn more about the company at www.ischemix.com.

    Julie-Ann Cabana
    Altasciences
    +1 514 601-9763
    jcabana@altasciences.com
     

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