Contract Pharma: Altasciences Acquires Sinclair Research

Altasciences Acquires Sinclair Research and Continues to Expand Preclinical Platform

Laval, Quebec, January 4, 2022 Altasciences, an integrated CRO/CDMO offering pharmaceutical and biotechnology companies a seamless solution to early-stage drug development from lead candidate selection to clinical proof of concept, announced today the completed acquisition of Sinclair Research, a preclinical CRO located in the Midwest. Complementing existing locations on the East and West Coast, the new site will facilitate even greater access to Altasciences’ preclinical services across the U.S.

This acquisition will add significant capacity and expertise to Altasciences’ existing preclinical offering,” said Steve Mason, Co-Chief Operating Officer at Altasciences. “Sinclair’s experience conducting research on a wide variety of species in a comprehensive range of drug classes will broaden our current preclinical offering and support Altasciences’ focus on providing our clients with customized solutions.

With over 80 animal rooms, Sinclair Research is a large nonclinical CRO in the U.S.A. providing full-service IND and NDA-enabling toxicology and safety pharmacology services. Built on more than 50 years of experience, Sinclair Research provides services to support biopharmaceutical, animal health, and medical device development programs. “We are very excited to be joining the Altasciences team, and look forward to being able to offer our preclinical services to a broader market by leveraging the resources and expertise of an integrated, global CRO,” stated Guy Bouchard, Chief Executive Officer at Sinclair Research. 

With this acquisition, Altasciences is continuing to advance its strategic growth plan to provide an expanded range of services in support of our integrated early-phase drug development solutions. Sinclair Research shares our commitment to animal welfare, and we look forward to merging our talents and working together with our new team of preclinical experts in the Midwest,” added Chris Perkin, Altasciences’ Chief Executive Officer.

Fredrikson & Byron P.A. and Goodwin Procter LLP served as legal advisors to Altasciences on the transaction. Fairmount Partners acted as exclusive financial advisors to Sinclair, and Troutman Pepper acted as legal counsel.

 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.

CONTACT:
Julie-Ann Cabana
Altasciences
514 601-9763
jcabana@altasciences.com

In 2021, you did incredible things — and we are grateful to have been part of your journey.

Top Scientific Resources of 2021

Top Scientific Resources of 2021

With the year coming to an end, we rounded-up some of our most insightful scientific resources from 2021. Check out what you may have missed, discover more about our areas of expertise, and learn how we can help you accelerate your drug development program.

Preclinical
1.





 
The Altascientist: Planning your Preclinical Assessment for a Successful Regulatory Submission
A thorough review of IND requirements and preclinical program considerations, including a guide to help you estimate small molecule and biologic timelines.
Read More
 
2.



 
The Altascientist: Safety Pharmacology Guidelines and Practices – A Review
How to reduce the use of test animals, save time, and ensure quality data. Read More
 
3.




 
Podcast: Consultant Series ― A chat with Dr. John Atkinson, Founder of Atkinson Toxicology Consulting
Dr. Atkinson’s journey in the drug development industry, his experience as the former president of the American College of Toxicology, what to look for in a CRO partner, and much more. Listen Now
Clinical
4.


 
The Altascientist: Planning your First-in-Human Trial
A thorough review of the first-in-human clinical trial process, including planning and conduct. Read More
 
5.



 
Blog: Ethnobridging Supports Global Clinical Development
Historical background on ethnobridging and how it developed into a mainstream strategy. Learn More
 
6.




 
Webinar: The Brain on Drugs: The Strategic Use of Cognitive Measures and Biomarkers in Early-Phase CNS Drug Studies 
Key clinical and bioanalytical considerations when it comes to pharmacokinetics and pharmacodynamics data specific to biologics. Watch Now
Manufacturing
7.




 
E-Book: Liquid-Filled Capsules: Getting Your Drug to the Clinic – FAST
How liquid-filled, hard-shell capsules can help accelerate drug development programs and entry into clinical trials. Read More
 
8.




 
The Altascientist: Terminal Sterilization of Pharmaceutical Products
Why regulatory agencies, such as the FDA and EMA, prefer terminal sterilization over aseptic processing. Learn More
 
9.


 
Webinar: Overcoming the Challenges of Manufacturing and Clinical Trials
An overview of our pharmacy and manufacturing services, including a recent case study. Watch Now
Bioanalytical
10.





 
Webinar: Patient Centricity and the Evolving Role of Microsampling
An in-depth bioanalytical and clinical exploration of microsampling technology and its significance in supporting patient-centric healthcare initiatives, along with case studies to demonstrate.  Watch Now
 
11.




 
Insert: Flow Cytometry Solutions to Support your Preclinical and Clinical Studies
An overview of our flow cytometry services, on-site equipment, flow markers, and NHP panels to support your preclinical and clinical studies. Read More
 
12.



 
Infographic: The Key To Selecting The Right Bioanalytical Platform For Your Molecule
How to expedite your research goals by proactively selecting the best pathway for your unique molecule. Learn More
Research
13.




 
Quick Chat: A Seamless Experience, Thanks to Expert Scientific Project Management
An inside look at Altasciences' Scientific Project Management team, our company culture, and how we assign project and program managers. Watch Now
 
14.


 
Webinar: Demystifying the CTA Process in Canada
Benefits of conducting FIH trials in Canada for biopharmaceutical companies. Watch Now
 
15.



 
Interview: Five Things to Know About Scientific Affairs
Catherine Dussault, Director of Scientific Affairs, discusses how her team is able to design and conduct the most appropriate study for each unique development program. Read More

Have five more minutes? You may be interested in:


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 from lead candidate selection to clinical proof of concept, and beyond.

Virpax Announces Clinical Trial Site in Canada for First in Human Study of Epoladerm™ for Pain Associated with Osteoarthritis of the Knee

December 2021

In this issue

Complimentary industry webinars and podcasts, thought-provoking articles, industry news, and more!

Access Full Newsletter


The Altascientist: Scientific Journal

Read the latest issue: “Psychedelics and Entactogens: Challenges Associated with Schedule I Therapeutics”.


Four Reasons to Choose Altasciences as Your Flow Cytometry Partner

Given the highly specialized nature of flow cytometry testing and the unique set of competencies required to carry it out, choosing the right partner is key to ensuring a successful study.


Psychedelics — Regulatory Environment Challenges

In the past, stigmatization and criminalization have blocked psychedelics from realizing their full potential in medicine and scientific research. Now, with growing research and education, this is all changing. In this article, we explore the past, present, and future regulatory environment for Schedule I therapeutic development.


Citeline Awards Names Altasciences as a Finalist for Best Sponsor-facing Technology Initiative of 2021

Altasciences was shortlisted for its proprietary database, Ask Albert. Ask Albert is behind our commitment to fueling integration and facilitating information-sharing across departments and sites, so that you only have to Tell Us Once™.


Respira Technologies, Inc. Chooses Altasciences to Manufacture World's First Inhaled Nicotine Replacement Therapy (NRT)

Altasciences’ CDMO site in Philadelphia, PA will manufacture the world’s first FDA-approved inhaled smoking cessation therapy. This treatment uses RespiRx™, a vibrating mesh nebulizer (VMN) with a disposable cartridge that is maintenance-free, reliable, and eliminates the risk of patient misuse.


Global Business Reports Interviews Altasciences’ CEO

In a one-on-one interview with GBR, Chris Perkin discusses Altasciences’ place in early phase drug development, the company’s evolution, and its vision for the industry.


XORTX Therapeutics Partners with Altasciences for Clinical Study on Kidney Disease Treatment

The clinical study is in support of developing a treatment for autosomal dominant polycystic kidney disease (ADPKD) and for acute kidney injury associated with Coronavirus infection.


CDMO Expansion Continues with Additional Facilities in Philadelphia

Contract Pharma reports on the continuing expansion of Altasciences’ CDMO site, specifically the launch of a second client-dedicated building project. 


Altasciences Contributes to the Clinical Development of Bisoprolol/Ramipril Fixed-Dose Combination

Read about the study findings of three studies conducted at Altasciences in this article published in Clinical and Translational Science.


Up Close and Personal with… Dr. Denise Milovan

Meet Altasciences’ Scientific Manager, Biostatistics, Data Services, at Altasciences.


Moving Your Drug Forward to Preclinical Trials

Discover key considerations when planning to transition from drug discovery to preclinical trials.


The Next Trip: Developing the Second Generation of Psychedelics and Their Analogs for Targeted Medical Use

Read about how, after years of stagnation, this field of research is being revitalized by the investigation of their potential benefit of mainstream psychiatric applications.


BEFORE YOU GO:

  • Webinars
    Watch (or re-watch) our latest on-demand webinars and podcast episodes, including the second episode of “The Many Faces of Recreational Drug Use” and a new webinar, “Overcoming Bioanalytical Challenges of PK/PD Assessment in Phase I Biologics Studies”.  
  • Quick Chats
    Get to know the people and the approach that make Altasciences a different kind of CRO/CDMO with these short video interviews featuring some of our experts and team leaders.
  • Upcoming Events
    See what events we’ll be attending over the new few weeks.

Are You Looking for Help with Scientific Publications?

 

Scientific Publication Writing — Let Us Help!

Altasciences’ scientific experts can provide you with strategic guidance and quality writing for your next scientific publication. Our solution includes writing for a wide range of therapeutic areas, for your preclinical to clinical research — as part of a full‑service program completed at our facilities or as a stand-alone offering.
 
Benefit from: 

  • Strategic publication guidance and content development for manuscripts, posters, and abstracts
  • Expert review and editing of your pre-written publications
  • And more!

Let’s get started!

Have 5 minutes? You may be interested in:

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 from lead candidate selection to clinical proof of concept, and beyond.

FDA and EMA Prefer Terminal Sterilization Over Aseptic Manufacturing ― Find Out Why

 

Advantages of Terminal Sterilization Over Aseptic Manufacturing

Regulatory agencies such as the FDA and EMA generally prefer terminal sterilization over aseptic manufacturing, as it provides a high level of sterility assurance. It is also less complex, less costly, more easily reproducible than aseptic manufacturing, and offers time savings to pharmaceutical companies.

In this issue of The Altascientist, we discuss:

  • Differences between terminal sterilization and aseptic manufacturing 
  • Sterilization methods for pharmaceutical products
  • Validation steps during sterilization
  • Method selection 

Read to learn how terminal sterilization can benefit your drug product. 

Altascientist Issue 21

Questions? Speak with one of our experts? Contact Us.

Proactive Investors: Emyria's Ultra-Pure CBD Capsule Outperforms TGA-Approved CBD Treatment in Pre-Clinical Animal Trial

Drug Discovery World: Pharmacokinetic Study for Developing Kidney Disease and Injury Therapies

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