Company profile for Astellas Pharma

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About

Astellas Pharma Inc., to fulfill its business philosophy to "Contribute toward improving the health of people around the world through the provision of innovative and reliable pharmaceutical products," is actively engaged in business as an R&D-driven global pharmaceutical company. We wish to be of help to each patient who is fighting illness by continuously generating innovative and highly beneficial drugs for diseases which ...
Astellas Pharma Inc., to fulfill its business philosophy to "Contribute toward improving the health of people around the world through the provision of innovative and reliable pharmaceutical products," is actively engaged in business as an R&D-driven global pharmaceutical company. We wish to be of help to each patient who is fighting illness by continuously generating innovative and highly beneficial drugs for diseases which high unmet medical needs exist, through continuous efforts in research and development, and providing them.

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CONTACT DETAILS

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Country
Country
Japan
Address
Address
2-5-1, Nihonbashi-Honcho, Chuo-Ku, Tokyo 103-8411
Telephone
Telephone
+81-3-3244-3000
youtube
YouTube

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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: 4916

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: 4560

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.prnewswire.com/news-releases/us-fda-confirms-class-1-resubmission-of-the-supplemental-new-drug-application-for-izervay-avacincaptad-pegol-intravitreal-solution-for-geographic-atrophy-302346418.html

PR NEWSWIRE
08 Jan 2025

https://www.prnewswire.com/news-releases/chinas-national-medical-products-administration-nmpa-approves-padcev-in-combination-with-keytruda-pembrolizumab-for-the-treatment-of-advanced-bladder-cancer-302345641.html

PR NEWSWIRE
08 Jan 2025

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/astellas-pharma-us-inc-issues-voluntary-nationwide-recall-one-lot-prografr-05mg-tacrolimus-and-one

FDA
24 Dec 2024

https://www.fiercebiotech.com/biotech/astellas-pays-sangamo-20m-upfront-improve-neurological-gene-therapy-capabilities

FIERCE BIOTECH
19 Dec 2024

https://www.businesswire.com/news/home/20241218204650/en

BUSINESSWIRE
19 Dec 2024

https://www.prnewswire.com/news-releases/astellas-and-sangamo-therapeutics-announce-capsid-license-agreement-to-deliver-genomic-medicines-for-neurological-diseases-302335494.html

PR NEWSWIRE
19 Dec 2024

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Tacrolimus

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Tacrolimus

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Tamsulosin

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Tamsulosin

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Cefixime

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Cefixime

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Famotidine

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Famotidine

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Micafungin

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Micafungin

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Cefazolin

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Cefazolin

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Formoterol Fumarate

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Formoterol Fumarate

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Rhizoxin

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Rhizoxin

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Zotepine

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Zotepine

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SYNTHESIS OF PYRROINITRIN

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SYNTHESIS OF PYRROINITRIN

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Drugs in Development

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Details:

Under the license agreement, Astellas will leverage Sangamo's novel proprietary neurotropic adeno-associated virus (AAV) capsid, STAC-BBB for the treatment of neurological diseases.


Lead Product(s): AAV based Gene Therapy

Therapeutic Area: Neurology Brand Name: Undisclosed

Study Phase: Discovery PlatformProduct Type: Cell and Gene therapy

Recipient: Sangamo Therapeutics

Deal Size: $1,320.0 million Upfront Cash: $20.0 million

Deal Type: Licensing Agreement December 19, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Under the license agreement, Astellas will leverage Sangamo's novel proprietary neurotropic adeno-associated virus (AAV) capsid, STAC-BBB for the treatment of neurological diseases.

Brand Name : Undisclosed

Molecule Type : Cell and Gene therapy

Upfront Cash : $20.0 million

December 19, 2024

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IZERVAY (avacincaptad pegol intravitreal solution), a complement C5 inhibitor for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).


Lead Product(s): Avacincaptad Pegol

Therapeutic Area: Ophthalmology Brand Name: Izervay

Study Phase: ApprovedProduct Type: Large molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 19, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : IZERVAY (avacincaptad pegol intravitreal solution), a complement C5 inhibitor for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).

Brand Name : Izervay

Molecule Type : Large molecule

Upfront Cash : Not Applicable

November 19, 2024

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Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.


Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine

Therapeutic Area: Oncology Brand Name: Vyloy

Study Phase: ApprovedProduct Type: Large molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 21, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.

Brand Name : Vyloy

Molecule Type : Large molecule

Upfront Cash : Not Applicable

October 21, 2024

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Astellas receives an exclusive option to license AVB-101, an investigational, AAV-based gene therapy in Phase 1/2 development for patients with frontotemporal dementia with progranulin mutations.


Lead Product(s): AVB-101

Therapeutic Area: Neurology Brand Name: AVB-101

Study Phase: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Recipient: AviadoBio

Deal Size: $2,230.0 million Upfront Cash: $50 million

Deal Type: Agreement October 08, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Astellas receives an exclusive option to license AVB-101, an investigational, AAV-based gene therapy in Phase 1/2 development for patients with frontotemporal dementia with progranulin mutations.

Brand Name : AVB-101

Molecule Type : Cell and Gene therapy

Upfront Cash : $50 million

October 08, 2024

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Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.


Lead Product(s): Enfortumab Vedotin,Pembrolizumab

Therapeutic Area: Oncology Brand Name: Padcev

Study Phase: ApprovedProduct Type: Large molecule

Sponsor: Pfizer Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 24, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.

Brand Name : Padcev

Molecule Type : Large molecule

Upfront Cash : Not Applicable

September 24, 2024

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Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.


Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine

Therapeutic Area: Oncology Brand Name: Vyloy

Study Phase: Phase IIIProduct Type: Large molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 20, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.

Brand Name : Vyloy

Molecule Type : Large molecule

Upfront Cash : Not Applicable

September 20, 2024

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Veozah (fezolinetant) is a neurokinin 3 (NK3) receptor antagonist being investigated for the treatment of vasomotor symptoms in patients with breast cancer.


Lead Product(s): Fezolinetant

Therapeutic Area: Obstetrics/Gynecology (Women’s Health) Brand Name: Veozah

Study Phase: Phase IIIProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 27, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Details : Veozah (fezolinetant) is a neurokinin 3 (NK3) receptor antagonist being investigated for the treatment of vasomotor symptoms in patients with breast cancer.

Brand Name : Veozah

Molecule Type : Small molecule

Upfront Cash : Not Applicable

August 27, 2024

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Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda, a PD-1 inhibitoris approved for locally advanced or metastatic urothelial cancer.


Lead Product(s): Enfortumab Vedotin,Pembrolizumab,Cisplatin

Therapeutic Area: Oncology Brand Name: Padcev

Study Phase: ApprovedProduct Type: Large molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 27, 2024

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BIO Partnering at JPM
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BIO Partnering at JPM
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Lead Product(s) : Enfortumab Vedotin,Pembrolizumab,Cisplatin

Therapeutic Area : Oncology

Highest Development Status : Approved

Partner/Sponsor/Collaborator : Not Applicable

Deal Size : Not Applicable

Deal Type : Not Applicable

Details : Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda, a PD-1 inhibitoris approved for locally advanced or metastatic urothelial cancer.

Brand Name : Padcev

Molecule Type : Large molecule

Upfront Cash : Not Applicable

August 27, 2024

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Details:

Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.


Lead Product(s): Enfortumab Vedotin,Pembrolizumab

Therapeutic Area: Oncology Brand Name: Padcev

Study Phase: ApprovedProduct Type: Large molecule

Sponsor: Pfizer Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 19, 2024

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BIO Partnering at JPM
Not Confirmed
BIO Partnering at JPM
Not Confirmed

Details : Padcev (enfortumab vedotin), a nectin-4 inhibitor ADC in combination with keytruda, a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.

Brand Name : Padcev

Molecule Type : Large molecule

Upfront Cash : Not Applicable

August 19, 2024

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Details:

Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.


Lead Product(s): Zolbetuximab,Oxaliplatin,Capecitabine

Therapeutic Area: Oncology Brand Name: Vyloy

Study Phase: Phase IIIProduct Type: Large molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 26, 2024

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BIO Partnering at JPM
Not Confirmed
BIO Partnering at JPM
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Details : Vyloy (zolbetuximab) is a chimeric IgG1 monoclonal antibody that binds to CLDN18.2. It is being evaluated for HER2-negative gastric or gastroesophageal junction adenocarcinoma.

Brand Name : Vyloy

Molecule Type : Large molecule

Upfront Cash : Not Applicable

July 26, 2024

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FDF Dossiers

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Brand Name : ADENOSCAN

BIO Partnering at JPM
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Brand Name : ADENOSCAN

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BIO Partnering at JPM
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Astellas Pharma

Dosage Form : SOLUTION;INTRAVENOUS

Brand Name : ADENOSCAN

Dosage Strength : 60MG/20ML (3MG/ML) **F...

Packaging :

Approval Date : 1995-05-18

Application Number : 20059

Regulatory Info : DISCN

Registration Country : USA

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Brand Name : ADENOCARD

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Brand Name : ADENOCARD

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BIO Partnering at JPM
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Astellas Pharma

Dosage Form : INJECTABLE;INJECTION

Brand Name : ADENOCARD

Dosage Strength : 3MG/ML **Federal Regis...

Packaging :

Approval Date : 1989-10-30

Application Number : 19937

Regulatory Info : DISCN

Registration Country : USA

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Brand Name : ADENOSCAN

BIO Partnering at JPM
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Brand Name : ADENOSCAN

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BIO Partnering at JPM
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Astellas Pharma

Dosage Form : SOLUTION;INTRAVENOUS

Brand Name : ADENOSCAN

Dosage Strength : 90MG/30ML (3MG/ML) **F...

Packaging :

Approval Date : 1995-05-18

Application Number : 20059

Regulatory Info : DISCN

Registration Country : USA

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04

Brand Name : Fosfalugel

BIO Partnering at JPM
Not Confirmed
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Brand Name : Fosfalugel

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form :

Brand Name : Fosfalugel

Dosage Strength : 26 Bust Gel Os 15 Ml 1...

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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05

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : CREAM;TOPICAL

Brand Name : CYCLOCORT

Dosage Strength : 0.025% **Federal Regis...

Packaging :

Approval Date : 1982-01-01

Application Number : 18116

Regulatory Info : DISCN

Registration Country : USA

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06

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : OINTMENT;TOPICAL

Brand Name : CYCLOCORT

Dosage Strength : 0.1% **Federal Registe...

Packaging :

Approval Date : 1982-01-01

Application Number : 18498

Regulatory Info : DISCN

Registration Country : USA

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07

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : CREAM;TOPICAL

Brand Name : CYCLOCORT

Dosage Strength : 0.1% **Federal Registe...

Packaging :

Approval Date : 1982-01-01

Application Number : 18116

Regulatory Info : DISCN

Registration Country : USA

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08

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : LOTION;TOPICAL

Brand Name : CYCLOCORT

Dosage Strength : 0.1%

Packaging :

Approval Date : 1988-06-13

Application Number : 19729

Regulatory Info : DISCN

Registration Country : USA

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09

Brand Name : Forcid Solutab 875/1...

BIO Partnering at JPM
Not Confirmed
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Brand Name : Forcid Solutab 875/1...

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : TAB

Brand Name : Forcid Solutab 875/125

Dosage Strength : 875mg

Packaging : 10X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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10

Brand Name : AMBISOME

BIO Partnering at JPM
Not Confirmed
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Brand Name : AMBISOME

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : POWDER FOR SOLUTION

Brand Name : AMBISOME

Dosage Strength : 50MG/VIAL

Packaging : 1/10 VIALS (20 OR 30 ML VIALS)

Approval Date :

Application Number : 2241630

Regulatory Info :

Registration Country : Canada

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FDA Orange Book

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01

Brand Name : ADENOCARD

BIO Partnering at JPM
Not Confirmed
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Brand Name : ADENOCARD

BIO Partnering at JPM
Not Confirmed
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Astellas Pharma

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ADENOCARD

Dosage Strength : 3MG/ML **Federal Registe...

Approval Date : 1989-10-30

Application Number : 19937

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Brand Name : ADENOSCAN

BIO Partnering at JPM
Not Confirmed
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Brand Name : ADENOSCAN

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : ADENOSCAN

Dosage Strength : 60MG/20ML (3MG/ML) **Fed...

Approval Date : 1995-05-18

Application Number : 20059

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Brand Name : ADENOSCAN

BIO Partnering at JPM
Not Confirmed
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Brand Name : ADENOSCAN

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : ADENOSCAN

Dosage Strength : 90MG/30ML (3MG/ML) **Fed...

Approval Date : 1995-05-18

Application Number : 20059

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : CREAM; TOPICAL

Proprietary Name : CYCLOCORT

Dosage Strength : 0.025% **Federal Registe...

Approval Date : 1982-01-01

Application Number : 18116

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

05

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : CREAM; TOPICAL

Proprietary Name : CYCLOCORT

Dosage Strength : 0.1% **Federal Register ...

Approval Date : 1982-01-01

Application Number : 18116

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
arrow

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : OINTMENT; TOPICAL

Proprietary Name : CYCLOCORT

Dosage Strength : 0.1% **Federal Register ...

Approval Date : 1982-01-01

Application Number : 18498

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

07

Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
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Brand Name : CYCLOCORT

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : LOTION; TOPICAL

Proprietary Name : CYCLOCORT

Dosage Strength : 0.1%

Approval Date : 1988-06-13

Application Number : 19729

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

Brand Name : AMBISOME

BIO Partnering at JPM
Not Confirmed
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Brand Name : AMBISOME

BIO Partnering at JPM
Not Confirmed
arrow

Astellas Pharma

Dosage Form : INJECTABLE, LIPOSOMAL; INJECTI...

Proprietary Name : AMBISOME

Dosage Strength : 50MG/VIAL

Approval Date : 1997-08-11

Application Number : 50740

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

Brand Name : IZERVAY

BIO Partnering at JPM
Not Confirmed
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Brand Name : IZERVAY

BIO Partnering at JPM
Not Confirmed
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Astellas Pharma

Dosage Form : SOLUTION; INTRAVITREAL

Proprietary Name : IZERVAY

Dosage Strength : EQ 2MG BASE/0.1ML (EQ 2M...

Approval Date : 2023-08-04

Application Number : 217225

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

Brand Name : CEFIZOX

BIO Partnering at JPM
Not Confirmed
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Brand Name : CEFIZOX

BIO Partnering at JPM
Not Confirmed
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Astellas Pharma

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFIZOX

Dosage Strength : EQ 500MG BASE/VIAL

Approval Date : 1983-09-15

Application Number : 50560

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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Europe

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01

Brand Name : Fosfalugel

BIO Partnering at JPM
Not Confirmed
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Brand Name : Fosfalugel

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form :

Dosage Strength : 26 Bust Gel Os 15 Ml 12.38 ...

Packaging :

Brand Name : Fosfalugel

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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02

Brand Name : Ridaura

BIO Partnering at JPM
Not Confirmed
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Brand Name : Ridaura

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Auranofina 3Mg 30 Joined' Oral...

Dosage Strength : 30 cpr riv 3 mg

Packaging :

Brand Name : Ridaura

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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03

Brand Name : Ipine

BIO Partnering at JPM
Not Confirmed
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Brand Name : Ipine

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Barnidipina 10Mg 28 Combined O...

Dosage Strength : 28 cps 10 mg modified relea...

Packaging :

Brand Name : Ipine

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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04

Brand Name : Ipine

BIO Partnering at JPM
Not Confirmed
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Brand Name : Ipine

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Barnidipina 20Mg 28 Combined O...

Dosage Strength : 28 cps 20 mg modified relea...

Packaging :

Brand Name : Ipine

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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05

Brand Name : Levact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Levact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Bendamustina 100Mg 5 Units Par...

Dosage Strength : 5 VIALS EV 100 mg 2,5 mg/ml

Packaging :

Brand Name : Levact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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06

Brand Name : Levact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Levact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Bendamustina 25Mg 20 Joined Th...

Dosage Strength : 20 VIALS EV 25 mg 2.5 mg/ml

Packaging :

Brand Name : Levact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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07

Brand Name : Levact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Levact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Bendamustina 25Mg 5 Units Pare...

Dosage Strength : 5 VIALS EV 25 mg 2.5 mg/ml

Packaging :

Brand Name : Levact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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08

Brand Name : Levact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Levact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Powder to concentrate to the i...

Dosage Strength : 2.5 mg/ml

Packaging : Hood glass

Brand Name : Levact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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09

Brand Name : Levact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Levact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : Powder to concentrate to the i...

Dosage Strength : 2.5 mg/ml

Packaging : Hood glass

Brand Name : Levact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Norway

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10

Brand Name : Ribovact

BIO Partnering at JPM
Not Confirmed
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Brand Name : Ribovact

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BIO Partnering at JPM
Not Confirmed

Astellas Pharma

Dosage Form : PULVER TILL KONCENTRAT TILL

Dosage Strength : 2,5 MG/ML

Packaging :

Brand Name : Ribovact

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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Astellas Pharma is a supplier offers 40 products (APIs, Excipients or Intermediates).

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