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BioWorld - Saturday, January 10, 2026
Home » Authors » Lee Landenberger

Articles by Lee Landenberger

Head to head: Beigene’s BTK inhibitor yields solid data against Imbruvica

April 28, 2021
By Lee Landenberger
Beigene Ltd.’s selective inhibitor, Brukinsa (zanubrutinib), made up for a 2019 miss in a head-to-head study against Johnson & Johnson and Abbvie Inc.’s Imbruvica (ibrutinib) with positive new data from a phase III trial in adults with relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma.
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Novavax-Oxford malaria vaccine has 77% efficacy in children

April 27, 2021
By Lee Landenberger
New phase IIb clinical trial data show the antigen R-21, a malaria vaccine candidate created by the University of Oxford that uses Novavax Inc.'s Matrix-M adjuvant, demonstrated 77% efficacy in children.
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Gold dollar sign

Arch Oncology’s CD47 antibody bolstered by a $105M series C

April 27, 2021
By Lee Landenberger
Being in a crowded space doesn’t bother recently installed Arch Oncology Inc. CEO Laurence Blumberg. As a matter of fact, he’s reassured by it. “There’s a lot of competition in CD47, that’s correct,” Blumberg told BioWorld. “But having been in industry for a long time, competition and the magnitude of that competition in pursuit of a target usually means there’s a good reason for that interest and that there’s compelling evidence it has utility.”
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Reviva’s stock revives with strong phase II data in schizophrenia

April 26, 2021
By Lee Landenberger
One of the keys to making a schizophrenia drug work is reducing the side effects, which, if they are powerful enough, will often cause patients to cease the treatment. Laxminarayan Bhat, Reviva Pharmaceuticals Holdings Inc.’s CEO, told BioWorld that new phase II data of the company’s lead candidate shows the drop-out rate was low compared to other schizophrenia drugs.
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Novavax-Oxford malaria vaccine has 77% efficacy in children

April 23, 2021
By Lee Landenberger
New phase IIb clinical trial data show the antigen R-21, a malaria vaccine candidate created by the University of Oxford that uses Novavax Inc.'s Matrix-M adjuvant, demonstrated 77% efficacy in children.
Read More

Like a rock: Obsidian and Vertex enter a gene editing deal worth up to $1.3B

April 22, 2021
By Lee Landenberger
After cutting a deal worth up to $1.1 billion with Crispr Therapeutics AG, it took Vertex Pharmaceuticals Inc. only two days to come up with another collaboration that could top the $1 billion mark, this time with Obsidian Therapeutics Inc.
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Test tubes with blood samples

Vertex and CRISPR in a $1.1B deal to develop sickle cell, beta-thalassemia therapy

April 20, 2021
By Lee Landenberger
In biotech and biopharma’s third-largest ever up-front development and commercialization deal, Crispr Therapeutics AG will receive an initial $900 million in an amended deal with Vertex Pharmaceuticals Inc. to lead the development, manufacturing and commercialization of gene editing therapy CTX-001 for sickle cell disease and transfusion-dependent beta-thalassemia.
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Playing the long game: Adagio pursues COVID-19 monoclonal antibody development with a $336M series C

April 19, 2021
By Lee Landenberger
The race to tame COVID-19 has morphed from a sprint to a long game as companies continue their development to handle a pandemic that is becoming endemic to the planet. That’s the case with Adagio Therapeutics Inc. as it chases clinical studies and an emergency use authorization (EUA) for its monoclonal antibody, ADG-20, to treat and prevent COVID-19.
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Going public ticker

Recursion’s IPO set to be 2021’s second highest

April 16, 2021
By Lee Landenberger
Recursion Pharmaceuticals Inc. priced its IPO at a level that, with anticipated gross proceeds of $436.4 million, would make it 2021’s second largest biopharma IPO and the eighth largest ever. Salt Lake City-based Recursion’s shares (NASDAQ:RXRX) were priced at $18 each when the market opened and closed April 16’s trading 73.89% higher at $31.30 each.
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Patient in hospital bed

Home and hospital: Merck-Ridgeback halt and advance COVID-19 study for different patient groups

April 15, 2021
By Lee Landenberger
Merck & Co. Inc. has shut down two COVID-19 therapy development studies while moving another into a phase III trial.
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