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Biotech Showcase 2025

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Biotech Showcase 2025

San Francisco, CA, United States | 13 January 2025 - 15 January 2025
Overview

Planning to attend Biotech Showcase 2025 in San Francisco? Schedule a partnering meeting with our expert to talk one-on-one about your drug development needs.

Meet Katie Stuart, Senior Director of Business Development, at the event. Katie is ready to hear about your drug program's challenges and discuss how Quotient Sciences can assist in accelerating your drug development timeline with our integrated approach.

Learn how our capabilities are fully integrated with our global drug product and clinical testing capabilities to further streamline your program. Our seamless integration of services has been proven to reduce at least 12 months of development time and substantially reduce R&D costs.

You can schedule a partnering meeting with us through the Biotech Showcase website/app or by using our form below.
 

Request
Location
Hilton Union Square
333 O'Farrell St, CA 94102
San Francisco, CA, United States

Fierce Biotech 2025

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Fierce Biotech 2025

San Francisco, United States | 14 January 2025 - 15 January 2025
Overview

Connect with us at Fierce Biotech 2025 this January

At Fierce JPM Week 2025, industry leaders will come together to explore what’s next. From market analysis to an examination of evolving regulatory landscapes, this event will provide expert insights into the opportunities and pressing challenges shaping the future of pharma, biotech, and healthcare.

fierce biotech cro award finalist 2024

 

If you are planning on attending, schedule a partnering meeting with Quotient Sciences to talk one-on-one about your drug development needs.

Jamie Weishaar, VP, Global Commercial Drug Product will be at this event and is ready to hear about your drug program's challenges and discuss how Quotient Sciences can assist in accelerating your drug development timeline with our integrated approach.  Learn how our capabilities are fully integrated with our global drug product and clinical testing capabilities to streamline your program. Our seamless integration of services has been proven to reduce at least 12 months of development time and substantially reduce R&D costs.

You can schedule a partnering meeting with us through the form below.  
 

Request
Location
Hyatt Regency
5 Embarcadero Center , CA 94111
San Francisco, United States

Modelling and Simulation of the Effect of a Permeability Enhancer on the Absorption of a Poorly Permeable Compound

Scientific Poster , Salcaprozate sodium SNAC , Reduced PBPK Model , Paracellular Permeability

Modelling and Simulation of the Effect of a Permeability Enhancer on the Absorption of a Poorly Permeable Compound

6 November 2024
Overview

Compound A is highly soluble at physiological pH, highly bound to proteins (%PPB >99.9%) and has poor permeability (Caco-2 Papp < 1 nm/s). In dog, the volume of distribution is low (50 mL/kg), clearance is 0.835 mL/h/kg and a mono-exponential decline in plasma concentration is observed. An enteric coated solid oral dosage form of compound A was developed. 

Due to its negligible intestinal permeability, the permeability enhancer Salcaprozate sodium (SNAC) was incorporated into the formulation. One mechanism proposed to explain the action of permeability enhancers is the transient opening of intestinal tight junctions (during a time window of ~20 minutes), leading to a temporary increase of paracellular permeability [1].


The objective of this work was to develop a reduced PBPK model for the oral administration of compound A in dogs, focusing on the alteration of paracellular permeability caused by SNAC.

Download
Date
6 November 2024

Physiologically Based Biopharmaceutics Modelling of the Effect of a Permeability Enhancer on the Absorption of a Highly Soluble and Poorly Permeable Small Peptide in Humans

Scientific Poster , Modelling & Simulation , Sodium Salcaprozate SNAC , Oral Peptides , Peptide Drug Development , Pharmacokinetics

Physiologically Based Biopharmaceutics Modelling of the Effect of a Permeability Enhancer on the Absorption of a Highly Soluble and Poorly Permeable Small Peptide in Humans

6 November 2024
Overview

Compound A is a highly soluble, highly protein bound and poorly permeable small peptide. In preclinical species, distribution volume is low (cynomolgus monkey ~0.35 L, dog ~0.46 L). Transitioning to clinical settings where oral administration is preferred over parenteral routes, an enteric coated (EC) tablet was formulated for Compound A. 

Given its poor permeability, sodium salcaprozate (SNAC), a permeability enhancer, was incorporated into the formulation. SNAC is proposed to facilitate the opening of tight junctions within the small intestine, thereby promoting paracellular absorption [1]. It has been reported that in vivo dissolution of EC formulations might be delayed compared to their in vitro counterparts, which may influence exposure [2]. 

It was hypothesised that using Physiologically Based Biopharmaceutics (PBB) Modelling, focusing on the alteration of intestinal paracellular permeability induced by SNAC, and variability in enteric coating performance could explain the pharmacokinetics variability of compound A.

The aim of the study was to develop a PBB model of Compound A based on variable permeability changes caused by varying local lumen SNAC concentrations; and by incorporating different dissolution lag times, to explain the variability of the SNAC effect leading to variability in Compound A exposure

Download
Date
6 November 2024

Quotient Sciences Predicting Belumosudil Drug-Drug Interactions Using a Physiologically Based Pharmacokinetic Model

Scientific Poster , Belumosudil , Drug-drug interactions , CYP3A4 inhibitor itraconazole

Quotient Sciences Predicting Belumosudil Drug-Drug Interactions Using a Physiologically Based Pharmacokinetic Model

6 November 2024
Overview

Belumosudil is a selective inhibitor of Rho-associated protein kinase 2 (ROCK2) approved for treating chronic graft-versus-host disease (cGVHD) in adult and paediatric patients. In vitro incubations with human liver microsomes indicated that the metabolism of belumosudil involves various cytochrome P450 (CYP) isoforms: CYP3A4 responsible for 41.9% of belumosudil metabolism, with contributions from CYP2D6 (21.7%), CYP2C8 (14.2%), CYP1A2 (<5%), CYP2C19 (<5%) and uridine diphosphate glucuronosyltransferase (UGT)1A9 [1].


In a clinical study on drug-drug interactions (DDIs) [1], it was observed that the strong CYP3A4 inhibitor itraconazole (ITZ) led to a 25% increase in belumosudil exposure (AUC0-t), while the strong CYP3A4 and CYP2C8 inducer rifampicin (RIF) resulted in a 72% decrease in AUC0-t, compared to the exposure levels when belumosudil was administered alone.

Download
Date
6 November 2024

Quotient Sciences Recognized as a Finalist in the 2024 Fierce CRO Awards

Awards & Recognition

Quotient Sciences Recognized as a Finalist in the 2024 Fierce CRO Awards

Quotient Sciences Recognized as a Finalist in the 2024 Fierce CRO Awards

Quotient Sciences has been recognized as a finalist in two categories of the 2024 Fierce CRO Awards.

The Fierce CRO Awards celebrate exceptional achievements and innovations by Contract Research Organizations (CROs). These awards recognize CROs that have demonstrated outstanding performance, innovation, and leadership in delivering high-quality research and development services. 

Entries in the 2024 Fierce CRO Awards were judged on the ability of the applicant to demonstrate innovation, impact, measurable outcomes, sustainability, scalability, ethical and regulatory adherence. This includes:

  • The level of creativity and effectiveness in advancing research and development services within the life sciences sector
  • Evidence of tangible results and improvements, such as successful trials, enhanced data quality, or improved client satisfaction
  • The potential for long-term impact and the ability to apply successful practices on a broader scale
  • Commitment to maintaining high ethical standards and complying with relevant regulations

The company was recognized for its submissions to the Excellence in Client Service and Partnership category, highlighting recent work in partnership with companies including YourChoice Therapeutics and its leading YCT-529 candidate. YCT-529 is currently the only hormone-free birth control pill for men that researchers are testing in humans.

In the Innovative Solutions in Drug Development category, the company highlighted the impact of the company's Translational Pharmaceutics platform for integrated drug development to programs with Evecxia Therapeutics on EVX-101 and with Ensysce Biosciences on PF614-MPAR.

Translational Pharmaceutics® integrates real-time cGMP drug product manufacturing (including oral solid dosage forms, such as tablets and capsules), clinical testing, project management, data sciences, and related capabilities needed to fully execute a Phase I clinical trial with healthy volunteers. Combining services and expertise as both a CDMO and CRO into one program makes it easy for clients to complete their programs, while benefitting from a single project manager for the entire process with oversight of a cross-functional project team. Each year, Quotient Sciences are consistently a leading provider of Phase I clinical trials in the UK.

"Giving our customers direct lines of communication to subject matter experts and more integrated way to complete drug programs are two things that consistently set us apart from other CDMOs and CROs." said Thierry Van Nieuwenhove, CEO, Quotient Sciences. "I'm proud of our teams and the wealth of our scientific knowledge that we are able to showcase to the industry."

Winners will be announced in the Fierce CRO Report in December.

On-Demand: A Deep Dive Into the CMC, Technology and Financial Aspects of Successful Development of an Orally Delivered GLP-1

On-Demand Webinar , GLP1 , Oral Peptides , Dr. Andy Lewis

On-Demand: A Deep Dive Into the CMC, Technology and Financial Aspects of Successful Development of an Orally Delivered GLP-1

31 October 2024
Overview

Dr. Andrew Lewis, Chief Scientific Officer, and Dr. Andrew Parker, Senior Drug Development Consultant, explore the drug delivery challenge in this follow-up from the first in our series “Development of Orally Delivered GLP-1 Therapeutics…From Diabetes to Obesity and Beyond”.

Our experts talk through the bioavailability challenge and offer perspectives on how pharma have successfully addressed this through molecule design and optimization of drug product performance through iterative clinical assessment, before describing how the initial GLP-1 therapeutics have stimulated other drug developers to expand into analogous mechanisms of action and small molecule therapeutics.

In this webinar:

  • Learn about the biopharmaceutic considerations for oral GLP-1 peptide therapeutics and how industry has innovated to overcome them
  • Hear about the health economic considerations of oral peptide delivery
  • Get an overview of other developments outside GLP-1 peptides to address the obesity therapeutic area

Watch our on-demand recording and stay at the forefront of treatment advancements in this quickly evolving category.

Watch
Date
31 October 2024

Leveraging Real-Time Clinical Data to Deliver Certainty in Solubility Enhancement and Modified Release Development

Oral Drug Product Delivery at Quotient Sciences

Leveraging Real-Time Clinical Data to Deliver Certainty in Solubility Enhancement and Modified Release Development

12 December 2024
Overview

Drug product optimization is a critical development step that is common for most drugs that are progressing through today’s development pipelines to respond to suboptimal exposure profiles, to transition from an early development formulation to one suitable for chronic administration in patients, or as part of a life-cycle management strategy.

If you would like to register, please use this link.

Traditional drug product optimization processes take 12-18 months to complete and place significant emphasis on the predictive power of laboratory and preclinical assessments. This approach is a non-optimal working model necessitated by the multiple disciplines required to develop, make and test new formulations in humans.

In this presentation, John McDermott and Andrew Parker will describe how the application of Quotient Sciences’ Translational Pharmaceutics® to re-engineer this process has created a Rapid Formulation Development and Clinical Testing approach, using clinical data to improve decision-making and halve development timelines using case studies from over 300 delivered programs.

Key learning objectives:

  • Develop an understanding of Translational Pharmaceutics®
  • Hear how Translational Pharmaceutics® can be applied to rapidly develop new formulations and evaluate their clinical performance
  • Hear case studies in spray drying, lipid formulation development and modified release

If you would like to register, please use this link.

Times

Thursday 12th December, 2024
3pm BST/ 4pm CET

Quotient Sciences and Medicines for Malaria Venture announce dosing of first-ever long-acting injectable for malaria prevention to study volunteers

Customer Milestone , News & Announcements

Quotient Sciences and Medicines for Malaria Venture announce dosing of first-ever long-acting injectable for malaria prevention to study volunteers

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 First-in-human study explores a single injection that provides 3 months of protection

  • This is the first clinical trial for Quotient Sciences and Medicines for Malaria Venture (MMV) of MMV371, a long-acting injectable.
  • The injectable could offer up to 3 months of protection against all types of malaria.
  • If successful in clinical trials, the final product has the potential to be a game changer, offering an affordable, long-lasting option to protect people of all ages from malaria.
  • The trial is being administered at Quotient Sciences – Nottingham, UK clinic in healthy male and female volunteers.

Nottingham, United Kingdom and Geneva, Switzerland — 28 October 2024. Medicines for Malaria Venture (MMV) and Quotient Sciences have begun the first clinical trial for a long-acting injectable (LAI) preventive compound for malaria. The trial, conducted in healthy volunteers in Nottingham, UK, marks a significant step toward preventing malaria in endemic regions.

According to the World Health Organization, in 2022, there were 249 million malaria cases and 608,000 deaths globally with sub-Saharan Africa bearing 95% of this burden. Innovations in malaria prevention are essential to respond to this ongoing public health crisis. In this trial, MMV371, a derivative of atovaquone — already approved as part of atovaquone-proguanil (Malarone®), a medicine widely used by travellers to malaria-endemic areas — is being tested in an injectable form that could provide up to 3 months of protection with a single intramuscular dose.

First-in-human clinical trial

The trial is evaluating the drug’s safety, tolerability and pharmacokinetics, or how the body interacts with the medicine. The final injectable medicine will be a fixed-dose combination of MMV371 and a suitable partner drug — a strategy that reduces the likelihood of inducing resistant strains of malaria parasites. Another compound in MMV’s pipeline, MMV055, is a potential partner drug candidate and is expected to enter clinical development in 2025.

The study is evaluating different dose levels of MMV371 in adult volunteers. If approved, this new product could potentially play a key role in protecting against new infections from all malaria parasite species, including the two most common strains, Plasmodium vivax and Plasmodium falciparum, the most deadly form of malaria.

An innovative approach to malaria prevention

The new drug combination could also potentially clear asymptomatic malaria infections, a condition in which malaria parasites are present in the blood, but no symptoms appear. Addressing asymptomatic malaria is an important element of malaria elimination strategies as individuals who are infected but have no disease symptoms are unlikely to seek treatment, therefore contributing to ongoing disease transmission. Over time, this unchecked transmission can lead to the emergence and spread of drug-resistant malaria as the parasite is continuously exposed to various antimalarial drugs used in symptomatic individuals.

Pending positive outcomes of the study, clinical trials in malaria-endemic countries are expected to begin in 2026. The final product could be a vital tool suitable for broad populations and multiple malaria strains, with the potential to complement existing interventions such as vaccines; seasonal malaria chemoprevention (SMC), a highly effective preventive oral intervention administered mainly to children under 5; and ideally, intermittent preventive treatment of malaria in pregnancy. An LAI could be advantageous in regions where SMC campaigns cannot be deployed due to parasite resistance to the drugs currently used. “This trial brings us closer to our goal of offering a long-lasting, affordable solution for malaria prevention”, said Dr Stephan Chalon, Vice President of Experimental Medicine and Clinical Pharmacology at MMV.

Dr Nand Singh, Medical Director at Quotient Sciences, said “We are pleased to support MMV with the clinical development of the antimalarial drug MMV371. The potential to help protect against P. vivax and P. falciparum strains and help save human lives is something that we are proud to be part of. This project will provide the scientific evidence for the potential development of long-acting injectable anti-malarial treatment.”

Affordability and broad reach

With affordability a key requirement of its target product profile, the LAI is intended for all age groups, especially young and school-aged children, who are among the highest risk for malaria infection and death. The LAI’s affordability, single-dose administration and ability to prevent malaria cases and treat asymptomatic infections make it a potential game-changer for global malaria elimination efforts.

About MMV 

MMV is a Swiss-based not-for-profit organization working to deliver a portfolio of accessible medicines with the power to treat, prevent and eliminate malaria. Born in 1999, out of a need for greater health equity, we close critical gaps in research, development and access — working “end-to-end” to expand the use of existing antimalarials and innovate new compounds to protect public health. This starts with women and children.

It’s working. As of 2023, MMV-supported products have effectively protected or treated an estimated 680 million people and saved around 15.4 million lives. We cannot stop now. 

However, with a quarter of a billion malaria cases and more than 600,000 deaths reported in 2022, progress towards disease elimination has stalled. MMV is part of an ecosystem of partners determined to change this. Bringing public and private sector partners together, we pioneer new solutions that align with local and global health priorities and promote the equitable development of effective and affordable products that work to help end malaria and advance health for all. For more information, visit www.mmv.org. 

For press enquiries, contact: 

Doreen Akiyo Yomoah
Communications Manager, MMV
Phone +41 79 238 60 74
E-mail: [email protected] 

About Quotient Sciences

Quotient Sciences is a drug development and manufacturing accelerator providing integrated programmes and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients. Everything we do for our customers is driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast, because humanity needs novel therapeutic solutions, fast. Quotient Sciences has been recognized as a multi-year winner of the CRO Leadership Awards in 2021, 2022, and 2024 and of the CDMO Leadership Awards in 2023. For more information, visit quotientsciences.com.

For press enquiries, contact:

Erica Fearnley
Executive Director, Strategic Marketing at Quotient Sciences
[email protected] 

Rachael Heath
Senior PR Manager at RaMarketing & PR
[email protected]

MMV Disclaimer 

This document contains certain forward-looking statements that may be identified by words such as ‘believes’, ‘expects’, ‘anticipates’, ‘projects’, ‘intends’, ‘should’, ‘seeks’, ‘estimates’, ‘future’ or similar expressions, or by discussion of, among other things, vision, strategy, goals, plans, or intentions. It contains hypothetical future product target profiles, development timelines and approval/launch dates, positioning statements, claims and actions for which the relevant data may still have to be established. Stated or implied strategies and action items may be implemented only upon receipt of approvals including, but not limited to, local institutional review board approvals, local regulatory approvals, and following local laws and regulations. Thus, actual results, performances or events may differ from those expressed or implied by such statements.  We ask you not rely unduly on these statements. Such forward-looking statements reflect the current views of Medicines for Malaria Venture (MMV) and its partner(s) regarding future events, and involve known and unknown risks and uncertainties. MMV accepts no liability for the information presented here, nor for the consequences of any actions taken on the basis of this information. Furthermore, MMV accepts no liability for the decisions made by its pharmaceutical partner(s), the impact of any of their decisions, their earnings and their financial status.

Thierry Van Nieuwenhove Shares His Insights on Emerging Trends in the CDMO Industry

Articles & Publications , Thierry Van Nieuwenhove

Thierry Van Nieuwenhove Shares His Insights on Emerging Trends in the CDMO Industry

Thierry Van Nieuwenhove

In this article by Contract Pharma, Thierry Van Nieuwenhove, the CEO of Quotient Sciences discusses how the CDMO is positioning itself to stay ahead of the curve and what are the most significant trends in the CDMO industry. 

Thierry also talks about the business highlights from the past 12-24 months and how the Quotient Sciences is integrating new technologies and innovations in its processes.

Continue reading the full article or watching the video on Contract Pharma.

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