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BioWorld - Friday, January 9, 2026
Home » Topics » Immune, BioWorld

Immune, BioWorld
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Aravax secures $22M to close series B for peanut allergy therapy

Jan. 29, 2024
By Tamra Sami
After raising $20 million in a series B round in December 2022, Aravax Pty Ltd. has raised another $22 million to close out its series B round with $42 million that expands the syndicate with new investors Novartis Venture Fund, Breakthrough Victoria, Uniseed, Unisuper, and Agati Capital. The funds will take the company’s peanut allergy immunotherapy, PVX-108, through phase II trials.
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Aravax secures $22M to close series B for peanut allergy therapy

Jan. 29, 2024
By Tamra Sami
After raising $20 million in a series B round in December 2022, Aravax Pty Ltd. has raised another $22 million to close out its series B round with $42 million that expands the syndicate with new investors Novartis Venture Fund, Breakthrough Victoria, Uniseed, Unisuper, and Agati Capital. The funds will take the company’s peanut allergy immunotherapy, PVX-108, through phase II trials.
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Test tubes with blood samples

With series A funds, IMU Bio’s Cytatlas identifies cell types and immune signatures

Jan. 24, 2024
By Nuala Moran
IMU Biosciences Ltd. has raised £11.5 million (US$14.7 million) in a series A round to further develop and commercialize profiling technology that can identify from a blood sample which of more than 2,000 cell types are present in an individual’s immune system.
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IPO market picking up? CAR T firm Kyverna sixth firm to file for US listing in 2024

Jan. 17, 2024
By Jennifer Boggs
Kyverna Therapeutics Inc. disclosed a filing to raise up to $100 million in an IPO, becoming the sixth firm to announce plans for a U.S. listing in the new year, offering tentative hope that the public markets might prove more welcoming to biopharma firms after a lackluster 2023.
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Art concept for ancient DNA
Genetic/Congenital

MS? Blame great-great-great-great-great-great-great-great-grandma

Jan. 10, 2024
By Mar de Miguel
Current risk genes for some diseases such as multiple sclerosis (MS) may have emerged in the past as protection against infection by different pathogens. A group of researchers led by scientists from the University of Copenhagen has analyzed the ancient DNA of European populations and has revealed how MS, Alzheimer’s disease (AD) and diabetes arose as populations migrated. This evolution would explain the modern genetic diversity and the incidences of these pathologies observed today in the old continent.
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GC Biopharma scores FDA nod for immunoglobulin therapy Alyglo

Dec. 19, 2023
By Marian (YoonJee) Chu
South Korea’s GC Biopharma Corp. has gained U.S. FDA approval for its immune-deficiency plasma drug, Alyglo (immune globulin intravenous, human-stwk; IVIG-SN 10%), five months after refiling its BLA and before its PDUFA date of Jan. 13, 2024.
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ASH 2023: Syndax makes splash in cGVHD and leukemia

Dec. 12, 2023
By Brian Orelli
It’s not every day you see a small drug company’s presentations get picked for both the plenary session and the late-breaker session at a conference, but Syndax Pharmaceuticals Inc. managed to do just that at the 65th American Society of Hematology Annual Meeting 2023 – with a little help from a friend.
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CAR T cell with implanted gene strand

ASH 2023: CAR T therapies take on autoimmune diseases

Dec. 11, 2023
By Brian Orelli
CAR T-cell therapies have worked well at curing blood malignancies, but a group out of the University Hospital of Erlangen have repurposed the technology as a treatment for autoimmune diseases. The expansion into new diseases has required cooperation between multiple departments, with CAR T experts taking the lead on treatment and potential side effects, and rheumatologists measuring the outcomes of the treatment.
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Australian coins and bills

Mesoblast raising AU$97M for registration trials in GVHD, chronic back pain

Dec. 4, 2023
By Tamra Sami
Regenerative medicine company Mesoblast Ltd. plans to raise AU$97 million (US$64.5 million) to conduct additional phase III registration trials for its allogeneic stem cell treatment for steroid-refractory acute graft-vs.-host disease and for chronic back pain, as required by the U.S. FDA.
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Acelyrin: CRO’s vendor incorrectly programmed study protocol

Nov. 28, 2023
By Lee Landenberger
Acelyrin Inc. said a vendor used by Fortrea Inc., a CRO the company used for its phase IIb/III study testing interleukin-17A inhibitor izokibep in psoriatic arthritis, incorrectly programmed the study’s protocol and created a dose sequencing error, resulting in some patients in two of the four dosing arms to randomly receive placebo and active treatment instead of the intended alternating pattern. The discovery has prompted a review of other studies involving the CRO, including a study that failed to reach statistical significance in September.
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