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BioWorld - Saturday, June 20, 2026
Home » lymphoma

Articles Tagged with ''lymphoma''

Overland Pharma inks two JV agreements, building pipeline for Asian markets

Dec. 15, 2020
By Gina Lee
HONG KONG – Overland Pharmaceuticals Inc., a company created to bring innovative medicines to China, this week revealed the formation of two joint ventures intended to deliver on that mission, one with ADC Therapeutics SA and another with Allogene Therapeutics Inc.
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Dollar sign, up arrow

Trillium follows positive data and $25M equity investment with $130M offering

Sep. 11, 2020
By Lee Landenberger
Trillium Therapeutics Inc. is playing a hot hand. The immuno-oncology company followed recently revealed positive data from two dose-escalation phase I studies targeting CD47 by pulling down a $25 million equity investment from Pfizer Inc. Now the company has priced a $130 million underwritten public offering of 10 million common shares at $13 each.
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Leukemia illustration

Velosbio raises $137M series B for ROR1-targeting cancer therapies

July 8, 2020
By Michael Fitzhugh
Velosbio Inc., a San Diego-based company developing cancer therapies targeting receptor tyrosine kinase-like orphan receptor 1 (ROR1), has raised $137 million in series B financing to support development of its lead antibody-drug conjugate (ADC), VLS-101, and continued expansion of its pipeline.
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ASCO20: Allogene CAR T ‘shelf life’ mulled as early phase I results rival autologous

June 1, 2020
By Randy Osborne
Allogene Therapeutics Inc. investors will have to wait for an update in the second half of this year to find out more about whether off-the-shelf ALLO-501 can durably stand up to autologous CAR T-cell therapies, but early data disclosed at the American Society of Clinical Oncology meeting is creating buzz in the meantime.
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2-19-bionano-saphyr.png

Bionano Genomics sees encouraging results from study of Saphyr

Feb. 19, 2020
By Liz Hollis
The results from a study comparing San Diego-based Bionano Genomics Inc.’s Saphyr to traditional cytogenetic methods for the clinical analysis of leukemia genomes revealed that the system was 100% concordant with the standard of care for the detection of somatic chromosomal abnormalities.
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Gold chain link engraved with "partnership"
Up to $1.1B in milestones

Morphosys banks $750M up front plus $150M in stock sale as Incyte swoops in on tafasitamab

Jan. 13, 2020
By Cormac Sheridan
Ten days after its JAK1 inhibitor, itacitinib, failed a phase III trial in acute graft-vs.-host-disease (GVHD), Incyte Corp. has finalized a deal that could provide an alternative growth path. It is paying Morphosys AG $750 million up front, investing $150 million in its stock and is on the hook for up to $1.1 billion in milestones for a 50% interest in U.S. rights to the CD19-targeting antibody tafasitamab (MOR-208) and for 100% of the rights in all other territories.
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ASH 2019

Autolus’ CAR T therapy is well-tolerated

Dec. 9, 2019
By Lee Landenberger
ORLANDO, Fla. – New phase I/II data from Autolus Therapeutics plc announced at the American Society of Hematology’s (ASH) annual conference show that AUTO-3, the first bicistronic CAR T targeting CD19 and CD22 followed by an anti-PD1, was well-tolerated in a phase I/II study.
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ASH 2019

Genentech showcases new data on CD20-CD3 bispecific for tough-to-treat lymphomas

Dec. 9, 2019
By Michael Fitzhugh
ORLANDO, Fla. - Chimeric antigen receptor T (CAR T) cells have proved to be a major advance in treating patients with refractory B-cell malignancies so far. But, often, in approaching those issues "we solve one and we create another," Stephen Schuster, a doctor at the Abramson Cancer Center at the University of Pennsylvania in Philadelphia, told reporters at the 61st American Society of Hematology (ASH) annual meeting Saturday.
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FDA breast implant draft urges biennial MRI or ultrasound

Oct. 24, 2019
By Mark McCarty
The U.S. FDA's draft guidance for labeling and patient information for breast implants addresses concerns over anaplastic large cell lymphoma, but the draft also recommends biennial examination via ultrasound or MRI after five years, a recommendation that could prove a boon to makers of these imaging systems.
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