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BioWorld - Monday, April 6, 2026
Home » Topics » Immune, BioWorld

Immune, BioWorld
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Dragonfly expands Merck collaboration, adds new financing from Fidelity

March 19, 2020
By Michael Fitzhugh
Dragonfly Therapeutics Inc., of Cambridge, Mass., has expanded a strategic collaboration with Merck & Co. Inc. on the development of natural killer (NK) cell engager immunotherapies for oncology to add infectious disease and immune disorders. For $47.5 million up front, it's granting Merck the option to license exclusive rights to candidates developed using its TriNKET cell technology platform.
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Peanut allergy

Nuts! DBV to peel adhesive (red) tape from allergy bid; stock plunges

March 17, 2020
By Randy Osborne
DBV Technologies SA officials took pains to reassure investors that data wanted by the FDA with regard to the BLA for Viaskin Peanut allergy therapy are already in hand and need only be turned over to the agency, but that didn’t stop shares (NASDAQ:DBVT) from sliding 55.7%, or $2.93, to close March 17 at $2.33.
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Provention seeks to cure phase Ib antibody jitters; will lupus benefit PREVAIL?

March 12, 2020
By Randy Osborne
Anti-drug antibodies noted in the phase Ib portion of the PREVAIL study in lupus drew queries for Oldwick, N.J.-based Provention Bio Inc. during a conference call related to earnings, but analysts seemed more interested in the company’s later-stage push in type 1 diabetes (T1D).
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Medday’s confirmatory phase III in MS missteps

March 11, 2020
By Lee Landenberger
In a second phase III trial for treating progressive forms of multiple sclerosis (MS), designed to confirm the successful first trial, Medday Pharmaceuticals SA’s investigational MD-1003 failed to hit its primary and secondary endpoints.
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Two-year data buoy Hansa’s imlifidase MAA as CHMP decision looms

March 9, 2020
By Cormac Sheridan
DUBLIN – Hansa Biopharma AB is nearing a key milestone in its evolution, as a regulatory decision on its first marketing authorization application (MAA) looms. The EMA’s Committee for Medicinal Products for Human Use (CHMP) is expected to deliver an opinion during the second quarter on its application for imlifidase in supporting kidney transplants in sensitized patients.
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Harbour, Mount Sinai partner to develop Mabs targeting cancer, immunology and coronavirus

March 9, 2020
By David Ho
HONG KONG – U.S., China and the Netherlands-based Harbour Biomed Therapeutics Ltd. has teamed up with Mount Sinai Health System, New York City's largest academic medical system, to develop novel biotherapies in oncology and immunology. The two parties will also be using Harbour’s H2L2 Harbour Mice platform to develop a monoclonal antibody (MAb) against the coronavirus that has turned into a global epidemic.
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Onzeald to potter’s field, Nektar bempeg plans revealed

March 6, 2020
By Randy Osborne
During its Feb. 27, 2020, conference call on the previous year’s fourth-quarter results – though not in a related press release – Nektar Therapeutics Inc. let news drop that the prospective breast cancer (BC) therapy Onzeald (etirinotecan pegol) for patients with brain metastases had failed in top-line phase III outcomes.
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Kadmon TCT data provide ‘Incyte,’ GVHD odds looking better

Feb. 27, 2020
By Randy Osborne
New York-based Kadmon Holdings Inc.’s recent oral late-breaker session on KD-025 in chronic graft-vs.-host disease (cGVHD) at the Transplantation & Cellular Therapy (TCT) meeting – along with data that rolled out from two studies testing competitor Jakafi (ruxolitinib) from Incyte Corp. – signaled potential advantages in the former’s candidate, already highly regarded.
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Shanghai, China, stock market illustration

Bio-Thera launches $241M pre-revenue IPO on Shanghai’s STAR; shares up 83% on debut

Feb. 21, 2020
By Elise Mak
BEIJING – Chinese biosimilar maker Bio-Thera Solutions Ltd., of Guangzhou, on Feb. 21 launched a pre-revenue listing on Shanghai’s STAR market, a Nasdaq-style tech board, to reap $241 million at a valuation of almost $2 billion. Its share price soared more than 83% during its first trading day.
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Hoth touts preliminary data on lupus skin disease candidate

Feb. 12, 2020
By Michael Fitzhugh
New York-based Hoth Therapeutics Inc. said preliminary preclinical data on a topical nanoparticle formulation of the endocannabinoid anandamide it licensed from Zylö Therapeutics Inc. represents "a positive step toward underlining the transformative potential" of the early stage therapy for the skin disease cutaneous lupus erythematous.
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