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BioWorld - Sunday, January 11, 2026
Home » Authors » Jennifer Boggs

Jennifer Boggs

Articles

ARTICLES

FDA Approved stamp

Janssen’s teclistamab becomes first FDA-approved BCMA bispecific for MM

Oct. 26, 2022
By Jennifer Boggs
The U.S. FDA cleared teclistamab from Janssen Pharmaceutical Cos. as the first bispecific antibody for treating patients with relapsed or refractory multiple myeloma (MM), joining other BCMA-targeted drugs, including an antibody-drug conjugate and CAR T therapies.
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Liver tumor treatment conceptual illustration

Approval at last, but can Astrazeneca’s tremelimumab hit Stride in liver cancer?

Oct. 24, 2022
By Jennifer Boggs
It’s been a long road, but Astrazeneca plc’s anti-CTLA4 antibody, tremelimumab, finally earned its first U.S. FDA nod, cleared for use in combination with anti-PD-L1 drug Imfinzi (durvalumab) to treat patients with unresectable hepatocellular carcinoma (HCC). The commercial impact of the dual checkpoint therapy, however, remains to be seen, as it goes up against Roche Holding AG’s combination of Avastin (bevacizumab) and Tecentriq (atezolizumab), which gained standard-of-care status in first-line HCC in 2021.
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Mirum cites ‘compelling dataset’ as it aims to expand Livmarli into PFIC

Oct. 24, 2022
By Jennifer Boggs
Mirum Pharmaceuticals Inc. plans to “move rapidly toward regulatory filings” to expand use of IBAT inhibitor Livmarli (maralixibat) into progressive familial intrahepatic cholestasis (PFIC), President and CEO Chris Peetz told investors during a conference call Oct. 24 to discuss the positive top-line results from the phase III March study, which not only hit its primary endpoint in patients with PFIC2 but showed statistical improvements in pruritis across a range of PFIC subtypes.
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Polymer illustration
Newco news

Bioengineering MVP? Valitor aims to build a better therapeutic

Oct. 21, 2022
By Jennifer Boggs
With roughly a decade of work behind it, Valitor Inc. is ready to put its Multivalent Polymer (MVP) platform to the test, having recently announced its presence with a $28 million series B round and appointment of biopharma veteran Steven Lo as CEO. The next step is IND-enabling studies for its lead ophthalmology candidate, with clinical testing slated to start in 2024.
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NGM looks to subanalyses, Merck option following GA phase II miss

Oct. 17, 2022
By Jennifer Boggs
Over the next two weeks, the team at NGM Biopharmaceuticals Inc. will be digging through the data from its phase II trial of complement 3 inhibitor NGM-621 in patients with geographic atrophy (GA) secondary to age-related macular degeneration, following reports of a top-line miss Oct. 17 and a severe reaction from investors, who sent shares (NASDAQ:NGM) plummeting 70.5% to close at $3.41.
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Clinical trial virtual display

Kalvista’s [in]Komplete study gives boost to Orladeyo blockbuster ambitions

Oct. 5, 2022
By Jennifer Boggs
Biocryst Pharmaceuticals Inc. caught some industry observers by surprise early in 2022 when it upped its peak sales estimate for Orladeyo (berotralstat), its oral therapy for prevention of hereditary angioedema attacks, from $500 million to $1 billion. But blockbuster status appears more attainable following the latest setback from a potential competitor, as safety concerns prompted Kalvista Pharmaceuticals Inc. management to ax its phase II study testing KVD-824 in prevention of HAE attacks.
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Human cell illustration

Cellarity adds $121M in series C to look beyond targets in cell-centric approach

Oct. 4, 2022
By Jennifer Boggs
At first glance, Cellarity Inc. might appear as one more company harnessing the computational power of AI and machine learning to boost drug discovery efforts. A closer look, however, reveals a different approach, one that looks at cells and cellular behavior to address disease rather than the traditional method of seeking out molecular targets.
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T cells

Abpro inks potential $1.75B deal with Celltrion for HER2+ cancer therapy

Sep. 27, 2022
By Jennifer Boggs
Abpro Corp. and Celltrion Healthcare Inc. entered a global partnership valued at up to $1.75 billion involving ABP-102, a bispecific antibody targeting HER2-positive cancers, a move Abpro CEO Ian Chan said would help “accelerate this type of therapy for patients in need.”
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T cells

Lava soars on $700M Seagen deal for EGFR Gammabody candidate

Sep. 26, 2022
By Jennifer Boggs
Shares of Lava Therapeutics NV rocketed by more than 90% Sept. 26 as the company disclosed a licensing deal with Seagen Inc. to develop and commercialize preclinical-stage EGFR-targeting bispecific candidate LAVA-1223, which comes with $50 million in up-front funding and up to a potential $650 million in milestones. It also adds further validation for harnessing gamma-delta T cells to treat cancer, an approach that is growing increasingly popular.
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T cells

Abpro inks potential $1.75B deal with Celltrion for HER2+ cancer therapy

Sep. 21, 2022
By Jennifer Boggs
Abpro Corp. and Celltrion Healthcare Inc. entered a global partnership valued at up to $1.75 billion involving ABP-102, a bispecific antibody targeting HER2-positive cancers, a move Abpro CEO Ian Chan said would help “accelerate this type of therapy for patients in need.” With ABP-102 in preclinical development, Abpro decided to start looking for a partner. HER2 is “one of the biggest targets in biotech, mostly relevant for breast, colorectal and gastric cancers,” Chan told BioWorld. “Celltrion happened to have a lot of experience in the space.”
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View All Articles by Jennifer Boggs

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