Company profile for Acacia Pharma

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About

Acacia Pharma is a hospital pharmaceutical company focused on the development and commercialization of new products aimed at improving the care of patients undergoing significant treatments such as surgery, other invasive procedures or cancer therapy. The Company has identified important and commercially attractive unmet needs in these areas that its product pipeline aims to address.

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CONTACT DETAILS

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Country
Country
United Kingdom
Address
Address
The Officers’ Mess, Royston Road, Duxford, Cambridge, CB22 4QH
Telephone
Telephone
+44 (0)1223 919760
Linkedin
Linkedin
youtube
YouTube
Twitter
Twitter

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INTERVIEW #SpeakPharma

[Sponsored by another company]
“Translational Pharmaceutics, our flagship platform for drug development, empowers our clients with unparalleled flexibility”
This week, SpeakPharma interviews Denise Sutton, Chief Operating Officer and Site Head at Quotient Sciences’ Nottingham facility in the UK. Quotient Sciences is a drug development and manufacturing accelerator that offers the innovative Translational Pharmaceutics platform to support customers in overcoming drug development challenges. Sutton has been with the company for over 25 years. In this interview, she provides insights into the evolution of Quotient Sciences’ Nottingham facility and discusses how the organization has transformed from a small 10-bed clinic to a comprehensive drug development campus with six GMP suites. She also shares her perspective on the company’s unique approach to integrating drug development services. HIGHLIGHTS// evolution of Quotient Sciences’ Nottingham facility/ unique approach to integrating drug development services How has the Nottingham site transformed from when it was founded, to what it is today? Initially, we were a small company with fewer than 50 employees, a 10-bed clinic, and a single lab. Over 90 percent of our work focused on gamma scintigraphic imaging (a diagnostic test that creates images of the body’s internal organs and tissues using gamma rays). Due to the short half-life radionuclides we used to label dosage forms, every product we manufactured had a limited time to be dosed. At the end of 1999, we moved our headquarters to a purpose-built, two-storey facility—now known as Trent House on our now much larger Nottingham campus. We built three good manufacturing practice (GMP) suites on the top floor and three clinical wards on the bottom floor. These were very early days that marked the start of our Translational Pharmaceutics platform. We continued to expand the range of scintigraphy applications we offered in response to changing customer requirements until, in 2008, when we approached the MHRA (UK’s Medicines and Healthcare products Regulatory Agency) with a new request. We asked if it might be possible to work at the same pace as we did in our scintigraphic imaging studies, but do so for conventional drug development, without the radiolabel. We explored the application of ICH Q8 Quality by Design (QbD) guidelines to introduce a compositional design space into the CMC section of our regulatory dossier. This officially created a methodology for applying the Translational Pharmaceutics platform, and we haven't looked back since. Today, we have expanded substantially. Our Nottingham site is a campus of five buildings. We have development and analytical labs, six GMP suites, six clinical wards with a total of 85 beds (where we conduct healthy volunteer phase 1 clinical studies), and many talented colleagues covering our spectrum of CRO and CDMO services. HIGHLIGHTS// officially created a methodology for applying the Translational Pharmaceutics platform/ development and analytical labs/ six GMP suites   How is Translational Pharmaceutics applied to drug development programs? We apply Translational Pharmaceutics across three core applications: first-in-human clinical studies, drug product optimization programs through rapid formulation development and clinical testing, and as a part of human ADME (absorption, distribution, metabolism, and excretion) programs. No matter how a client chooses to work with us to apply Translational Pharmaceutics, the benefits of using a single organization and project management team to integrate services lets our clients remain in control and one step ahead of the emerging data that impacts the success of their molecule. Over all these years, our flagship Translational Pharmaceutics platform for drug development has remained unchanged in the way it empowers our customers and offers them unparalleled flexibility. HIGHLIGHTS// three core applications/ benefits of using a single organization/ clients remain in control   What would you say are the key strengths of Quotient Sciences’ Nottingham site? How do you support customer programs? Nowhere else would a single project manager oversee such a broad spectrum of activities, let alone be expected to ensure seamless, timely progression across functions that in any other company (i.e. at other CDMOs or CROs) would be delivered through multiple operating areas or through the use of a combination of third-party vendors. The project managers do face challenges. But by working with the project team, they are able to anticipate, avoid, and mitigate any impact whenever necessary. We know that time is incredibly valuable for our customers. A project Gantt chart is our project management team’s guiding light. I believe our project management team is truly world-leading – they communicate well, show great compassion, and lead with integrity. I’m super proud of our high-performing, supportive, cross-functional teams that support our customers when they trust their molecules to us, and work collaboratively to deliver the best possible service. After 25 years at Quotient, I continue to really enjoy going to work. I am indebted to various colleagues for helping me continue to feel this way. HIGHLIGHTS// project management team is truly world-leading/ high-performing, supportive, cross-functional teams/ 25 years at Quotient  

Impressions: 4930

https://www.pharmacompass.com/speak-pharma/translational-pharmaceutics-our-flagship-platform-for-drug-development-empowers-our-clients-with-unparalleled-flexibility

Radio Compass
16 Dec 2024

VLOG #PharmaReel

[Sponsored by another company]

DATA COMPILATION #PharmaFlow

[Sponsored by another company]
BMS, J&J, Bayer lead 25,000+ pharma layoffs in 2024; Amylyx, FibroGen, Kronos Bio hit by trial failures, cash crunch
Since 2022, there has been a significant surge in layoffs by pharmaceutical and biotech companies. While this trend continued into 2024, the industry showed signs of stabilization in the last four months of the year with the pace of layoffs slowing down. Nonetheless, 2024 was a challenging year. Data compiled by PharmaCompass indicates that over 25,000 layoffs were announced in 2024, driven by economic pressures, failed clinical trials, and strategic pivots. Bristol Myers Squibb and Johnson & Johnson led the layoffs with about 2,300 job cuts each. Bayer announced elimination of 1,800 positions.  View Our Interactive Dashboard on Biopharma Layoffs in 2024 (Free Excel Available) US, Europe, China bear brunt of job cuts; Big Pharma hands pink slips to 10,000 Over 190 biopharma companies announced layoffs in 2024. The year began on a grim note — 27 firms announced significant job cuts in January 2024. By the yearend, Big Pharma alone had contributed more than 10,000 layoffs to the year’s total of over 25,000. Novartis announced over 1,200 job cuts in 2024. It eliminated 330 jobs after it acquired German biotech MorphoSys through the closure of sites in Munich and Boston. Similarly, Bayer announced significant reductions at its US and Swiss facilities.  North America saw increased retrenchments, especially at biotech hubs such as Boston, San Diego, and New Jersey. Massachusetts, with Boston and Cambridge as the epicenter of US biotechnology, saw around 4,000 layoffs, with companies like Relay Therapeutics, Editas Medicine, and Takeda driving the numbers. In San Diego, workforce reductions by Takeda, and Bavarian Nordic collectively resulted in over 900 job losses, significantly impacting the local biotech ecosystem. New Jersey was subject to broader restructuring efforts with BMS and Bayer contributing nearly 1,500 layoffs. The impact in Europe was equally severe. Germany, home to some of the world’s largest pharmaceutical companies, saw over 2,500 layoffs as Bayer and Boehringer Ingelheim scaled back operations. Novartis’ decision to shut down its Munich site added hundreds more to the tally. In Switzerland, Idorsia eliminated 270 positions. Dutch biotech UniQure reduced its workforce by 65 percent (around 300 jobs). That included the sale of a Massachusetts manufacturing facility to Genezen. Denmark also felt the strain, with Leo Pharma cutting 250 roles as part of a strategic revamp. China emerged as another focal point of workforce reductions in 2024. Global pharmaceutical giants, such as Merck and Johnson & Johnson, restructured their operations in response to market complexities in the region. Local companies such as Connect Biopharma, which is transitioning to a US-focused company, also scaled back their presence in the country.  View Our Interactive Dashboard on Biopharma Layoffs in 2024 (Free Excel Available)  Amylyx, FibroGen, Lyra, Athira drastically reduce staff over setbacks in clinical trials Clinical trial failures were one of the most significant drivers of layoffs in 2024. For instance, Amylyx Pharmaceuticals faced a devastating blow when its amyotrophic lateral sclerosis (ALS) therapy, Relyvrio, failed a confirmatory trial. This led to a 70 percent reduction in its workforce, leaving only 100 employees from the 384 full-time staff reported at the end of 2023. The company’s decision to pull the therapy from the market compounded the layoffs. BioMarin Pharmaceutical had to reduce its workforce, as it streamlined its pipeline in response to trial challenges. In August, the company announced a reduction of 225 employees, citing “organizational redesign efforts”. These layoffs followed 170 redundancies announced earlier in May. FibroGen, once considered a leader in oncology drug development, was among the most heavily impacted. The high-profile failure of its anti-CTGF antibody in two late-stage cancer trials led to the discontinuation of its lead candidate, resulting in a 75 percent reduction in its US workforce. Lyra Therapeutics also implemented a 75 percent workforce reduction, affecting 87 employees, after its chronic rhinosinusitis program struggled. Similarly, Athira Pharma cut 70 percent of its team after its Alzheimer’s candidate failed a phase 2/3 trial.  View Our Interactive Dashboard on Biopharma Layoffs in 2024 (Free Excel Available)  Cash crunch, mergers compel Kronos Bio, Editas, Vincerx, Gilead to downsize In addition to clinical failures, funding constraints played a pivotal role in reshaping the biotech landscape. Kronos Bio stood out as one of the hardest-hit firms, cutting 21 percent and 83 percent of its existing workforce in March and November, respectively, as it sought to divest assets and conserve cash. Editas Medicine’s inability to secure partnerships for its sickle cell program forced the company to revert to preclinical research, resulting in a 65 percent workforce reduction. The trend of scaling back R&D pipelines was particularly evident among biotechs struggling to advance preclinical programs to clinical trials. Boundless Bio and Senti Bio exemplified this, choosing to focus on a handful of promising candidates, while reducing discovery efforts. Consolidation often results in overlapping roles, leading to inevitable workforce reductions. Apart from the MorphoSys layoffs by Novartis, Vincerx Pharma faced job losses after it got acquired by Oqory (a clinical-stage ADC company). Vincerx had to cut its workforce by 55 percent.  Amid ongoing reorganization efforts, Gilead closed its Seattle, Washington (US), office and laid off 72 employees of its subsidiary Kite Pharma. Gilead also announced that its Kite facility in Philadelphia, Pennsylvania (US), would close by mid-2025. That was followed by 104 additional layoffs at its California headquarters. In April, it had cut 58 jobs in California. Gilead also announced that its Kite facility in Philadelphia would close by mid-2025. Vir Biotechnology reduced its workforce by 25 percent (i.e. 140 layoffs) to focus on its hepatitis program, and GlycoMimetics let go of 80 percent of its workforce after the FDA demanded an additional clinical trial for its leukemia treatment. Meanwhile, Lexicon Pharmaceuticals reduced its workforce by 60 percent after it stopped commercial operations and transitioned back to being a clinical stage company.  View Our Interactive Dashboard on Biopharma Layoffs in 2024 (Free Excel Available)  Our view It takes decades to build innovation ecosystems. The concentration of layoffs in major biotech hubs has raised concerns about the potential long-term impact on these ecosystems. In 2025, the key challenge will be to maintain the momentum of innovation, as organizations operate with a leaner workforce and a more focused pipeline.  

Impressions: 4683

https://www.pharmacompass.com/radio-compass-blog/bms-j-j-bayer-lead-25-000-pharma-layoffs-in-2024-amylyx-fibrogen-kronos-bio-hit-by-trial-failures-cash-crunch

#PharmaFlow by PHARMACOMPASS
16 Jan 2025

NEWS #PharmaBuzz

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https://www.businesswire.com/news/home/20221110005491/en

BUSINESSWIRE
10 Nov 2022

https://www.globenewswire.com/news-release/2022/06/09/2459578/0/en/Eagle-Pharmaceuticals-Completes-Acquisition-of-Acacia-Pharma-Group-plc-Expanding-Acute-Care-Footprint.html

GLOBENEWSWIRE
09 Jun 2022

https://www.globenewswire.com/news-release/2022/06/07/2457505/0/en/Court-Sanction-of-the-Scheme-of-Arrangement.html

GLOBENEWSWIRE
07 Jun 2022

https://www.globenewswire.com/news-release/2022/05/20/2447445/0/en/Acacia-Pharma-Results-of-the-Court-Meeting-and-the-General-Meeting-held-on-19-May-2022.html

GLOBENEWSWIRE
20 May 2022
Publication of Scheme Document
Publication of Scheme Document

27 Apr 2022

// GLOBENEWSWIRE

https://www.globenewswire.com/news-release/2022/04/27/2429960/0/en/Publication-of-Scheme-Document.html

GLOBENEWSWIRE
27 Apr 2022

https://www.globenewswire.com/news-release/2022/03/31/2414158/0/en/Acacia-Pharma-Group-plc-Total-Number-of-Voting-Rights-and-Capital.html

GLOBENEWSWIRE
31 Mar 2022

Drugs in Development

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Details:

With the acquisition, addition of the two products expands the presence in acute care space, BARHEMSYS® (amisulpride for injection) and BYFAVO® (remimazolam for injection) join Eagle portfolio.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Eagle Pharmaceuticals

Deal Size: $182.4 million Upfront Cash: $78.5 million

Deal Type: Acquisition June 09, 2022

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01

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : With the acquisition, addition of the two products expands the presence in acute care space, BARHEMSYS® (amisulpride for injection) and BYFAVO® (remimazolam for injection) join Eagle portfolio.

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : $78.5 million

June 09, 2022

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Details:

Opportunity for Eagle’s highly skilled hospital-based salesforce to integrate and promote BYFAVO and BARHEMSYS and to leverage longstanding relationships to realize the full potential of these assets.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Eagle Pharmaceuticals

Deal Size: $182.4 million Upfront Cash: $78.5 million

Deal Type: Acquisition March 28, 2022

blank

02

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : Opportunity for Eagle’s highly skilled hospital-based salesforce to integrate and promote BYFAVO and BARHEMSYS and to leverage longstanding relationships to realize the full potential of these assets.

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : $78.5 million

March 28, 2022

blank

Details:

Barhemsys® is an intravenous formulation of amisulpride, a selective dopamine antagonist. It is approved in the US for treatment and prophylaxis of PONV, alone and in combination with other antiemetics.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 30, 2021

blank

03

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : Barhemsys® is an intravenous formulation of amisulpride, a selective dopamine antagonist. It is approved in the US for treatment and prophylaxis of PONV, alone and in combination with other antiemetics.

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : Not Applicable

September 30, 2021

blank

Details:

The net proceeds of the Placing are intended to be used To meet its sales force and marketing costs relating to BARHEMSYS® and BYFAVO™ including brand development and engagement with key opinion leaders, healthcare professionals and medical conference and speaker programs.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Undisclosed

Deal Size: $23.5 million Upfront Cash: Undisclosed

Deal Type: Financing February 18, 2021

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04

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : The net proceeds of the Placing are intended to be used To meet its sales force and marketing costs relating to BARHEMSYS® and BYFAVO™ including brand development and engagement with key opinion leaders, healthcare professionals and medical conference...

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : Undisclosed

February 18, 2021

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Details:

BYFAVO is the second Acacia Pharma product approved and launched in the US in the last year and extends its portfolio of new products targeting unmet needs in anesthesia.


Lead Product(s): Remimazolam Besylate

Therapeutic Area: Neurology Brand Name: Byfavo

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 28, 2021

blank

05

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : BYFAVO is the second Acacia Pharma product approved and launched in the US in the last year and extends its portfolio of new products targeting unmet needs in anesthesia.

Brand Name : Byfavo

Molecule Type : Small molecule

Upfront Cash : Not Applicable

January 28, 2021

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Details:

Under the Investment Agreement, Cosmo would have become eligible to receive a €5 million payment from the Company payable in new ordinary shares in the Company conditional upon the first commercial sale of the BYFAVO™ product in the United States.


Lead Product(s): Remimazolam Besylate

Therapeutic Area: Neurology Brand Name: Byfavo

Study Phase: ApprovedProduct Type: Small molecule

Recipient: Cosmo Pharmaceuticals

Deal Size: $45.0 million Upfront Cash: Undisclosed

Deal Type: Agreement December 15, 2020

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06

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : Under the Investment Agreement, Cosmo would have become eligible to receive a €5 million payment from the Company payable in new ordinary shares in the Company conditional upon the first commercial sale of the BYFAVO™ product in the United States.

Brand Name : Byfavo

Molecule Type : Small molecule

Upfront Cash : Undisclosed

December 15, 2020

blank

Details:

The Company plans to deploy this capital to support its ongoing US launches of BARHEMSYS® (amisulpride injection) for postoperative nausea & vomiting and BYFAVO™ (remimazolam for injection) for procedural sedation.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Cosmo Pharmaceuticals

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Financing October 09, 2020

blank

07

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : The Company plans to deploy this capital to support its ongoing US launches of BARHEMSYS® (amisulpride injection) for postoperative nausea & vomiting and BYFAVO™ (remimazolam for injection) for procedural sedation.

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : Undisclosed

October 09, 2020

blank

Details:

US DEA has designated its procedural sedative BYFAVO™ (remimazolam injection) as a Schedule IV medicine. This designation is the schedule for drugs with a low potential for abuse and low risk of dependence and is consistent with that granted to many other benzodiazepine drugs.


Lead Product(s): Remimazolam Besylate

Therapeutic Area: Neurology Brand Name: Byfavo

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 06, 2020

blank

08

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : US DEA has designated its procedural sedative BYFAVO™ (remimazolam injection) as a Schedule IV medicine. This designation is the schedule for drugs with a low potential for abuse and low risk of dependence and is consistent with that granted to many ot...

Brand Name : Byfavo

Molecule Type : Small molecule

Upfront Cash : Not Applicable

October 06, 2020

blank

Details:

BARHEMSYS® (amisulpride injection) has been launched and is now commercially available in the US for order and delivery to customers through major wholesalers and specialty distributors.


Lead Product(s): Amisulpride

Therapeutic Area: Gastroenterology Brand Name: Barhemsys

Study Phase: ApprovedProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 24, 2020

blank

09

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : BARHEMSYS® (amisulpride injection) has been launched and is now commercially available in the US for order and delivery to customers through major wholesalers and specialty distributors.

Brand Name : Barhemsys

Molecule Type : Small molecule

Upfront Cash : Not Applicable

August 24, 2020

blank

Details:

Acacia Pharma has been assigned the US license to BYFAVO™ (remimazolam) for injection by Cosmo Pharmaceuticals NV. BYFAVO for injection is a very rapid onset/offset intravenous benzodiazepine sedative for use during invasive medical procedures lasting 30 minutes or less.


Lead Product(s): Remimazolam Besylate

Therapeutic Area: Neurology Brand Name: Byfavo

Study Phase: ApprovedProduct Type: Small molecule

Recipient: Cosmo Pharmaceuticals

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement July 15, 2020

blank

10

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Acacia Pharma

United Kingdom
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

Details : Acacia Pharma has been assigned the US license to BYFAVO™ (remimazolam) for injection by Cosmo Pharmaceuticals NV. BYFAVO for injection is a very rapid onset/offset intravenous benzodiazepine sedative for use during invasive medical procedures lasting ...

Brand Name : Byfavo

Molecule Type : Small molecule

Upfront Cash : Undisclosed

July 15, 2020

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