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BioWorld - Sunday, December 7, 2025
Home » Astellas Pharma Inc.

Articles Tagged with ''Astellas Pharma Inc.''

Astellas reports positive results for roxadustat phase III study

June 10, 2020
By Gina Lee
HONG KONG – Astellas Pharma Inc. reported positive results from phase III of its DOLOMITES study comparing the efficacy and safety of roxadustat to that of darbepoetin alfa in treating anemia in nondialysis-dependent, stage 3 to 5 chronic kidney disease (CKD) patients.
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Prostate cancer cells

Two prostate cancer treatments in phase III prolong patient survival

May 14, 2020
By Lee Landenberger
New data show Johnson & Johnson’s Erleada (apalutamide) and Xtandi (enzalutamide) from Pfizer Inc. and Astellas Pharma Inc. both prolonged overall survival in men with non-metastatic castration-resistant prostate cancer (nmCRPC).
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Chess board and hybrid pawn

Astellas and Nanna Therapeutics ink $15M tie-up

April 28, 2020
By Gina Lee
HONG KONG – Not even the 9,500 kilometers between Cambridge, U.K., and Tokyo, or the ongoing COVID-19 pandemic, could prevent Japan’s Astellas Pharma Inc. from completing its acquisition of Cambridge-based Nanna Therapeutics Ltd. in a £12 million (US$14.78 million) deal.
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Chess board and hybrid pawn

Astellas and Nanna Therapeutics ink $15M tie-up

April 23, 2020
By Gina Lee
HONG KONG – Not even the 9,500 kilometers between Cambridge, U.K., and Tokyo, or the ongoing COVID-19 pandemic, could prevent Japan’s Astellas Pharma Inc. from completing its acquisition of Cambridge-based Nanna Therapeutics Ltd. in a £12 million (US$14.78 million) deal.
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Cancer cell, dropper, test tubes

Cytomx Probody language charms Astellas; tie-up potential $1.6B-plus

March 24, 2020
By Randy Osborne
Cytomx Therapeutics Inc. CEO Sean McCarthy told BioWorld that the longish hiatus between deals broken by the tie-up with Astellas Pharma Inc. was “very deliberate. Over that period of time, we were generating our first clinical data to get experience with how the technology works in cancer patients with our first two lead programs,” both of which have reached the phase II stage. A year ago in January, he said, the South San Francisco-based firm brought aboard Chief Business Officer Nick Galli to “hit the gas pedal a bit more in business development,” which led to the signing with Astellas, of Tokyo. Shares of Cytomx (NASDAQ:CTMX) closed March 24 at $6.53, up $1.60, or 32%.
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Handshake behind digital globe

Cytomx Probody language charms Astellas; tie-up potential $1.6B-plus

March 24, 2020
By Randy Osborne
Cytomx Therapeutics Inc. CEO Sean McCarthy told BioWorld that the longish hiatus between deals broken by the tie-up with Astellas Pharma Inc. was “very deliberate. Over that period of time, we were generating our first clinical data to get experience with how the technology works in cancer patients with our first two lead programs,” both of which have reached the phase II stage.
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Allo’, allo’, allo’: Adaptimmune, Astellas enter potential $897.5M allogeneic stem cell therapy pact

Jan. 14, 2020
By Cormac Sheridan
Adaptimmune plc continued its bright start to the year by entering an alliance worth up to $897.5 million with Astellas Pharma Inc. to co-develop and co-commercialize stem cell-based allogeneic CAR T and T-cell receptor (TCR) cell therapies.
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Kandy’s nonhormonal menopause therapy hits primary and secondary endpoints in phase IIb

Jan. 13, 2020
By Nuala Moran
LONDON – Kandy Therapeutics Ltd. has announced positive results for its nonhormonal treatment for menopause symptoms, showing a reduction in the number of hot flashes and night sweats, and a positive effect on secondary endpoints relating to mood and quality of life.
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Hand adding piece to puzzle

ConvertibleCARs ACCELerate with Astellas’ takeover of Xyphos; ‘tonneau’ potential in new approach?

Dec. 27, 2019
By Randy Osborne
Astellas Pharma Inc.’s early 2018 buyout of Universal Cells Inc. (UC) may have laid the groundwork for longer-range steps in allogeneic CAR T-cell therapy, but Xyphos Biosciences Inc. CEO James Knighton told BioWorld that the buyout of his firm provides the Tokyo-based giant for now with “an incredibly elegant solution that has tremendous potential.”
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FDA Approved stamp

FDA grants accelerated approval for Padcev to treat urothelial cancer

Dec. 19, 2019
By Lee Landenberger
A mere 26 months after the first patient was enrolled in its pivotal phase II study and about three months ahead of its PDUFA date, the FDA granted accelerated approval for Padcev (enfortumab vedotin-ejfv) to treat adults with locally advanced or metastatic urothelial cancer who have previously received a PD-1/L1 inhibitor and a platinum-containing chemotherapy before (neoadjuvant) or after (adjuvant) surgery or in a locally advanced or metastatic setting.
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