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BioWorld - Tuesday, March 3, 2026
Home » Authors » Caroline Richards

Articles by Caroline Richards

Vaccine and data illustration
Newco news

Baseimmune raises $11.3M to advance mutation-resistant vaccines

Feb. 27, 2024
By Caroline Richards
Baseimmune Ltd. has raised $11.3 million through a series A to accelerate the development of its deep learning AI technology for predicting future pathogen mutations to generate a series of longer-lasting, multistrain vaccines.
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EU flag, syringe, capsules

Sparsentan and two bird flu vaccines in EU positive opinion list

Feb. 23, 2024
By Caroline Richards
Seven new therapies, including two influenza vaccines, were recommended for approval by the EMA’s Committee for Medicinal Products for Human Use during its February 2024 meeting. One of these was sparsentan by CSL Vifor Pharma Inc. and Travere Therapeutics Inc. for the treatment of IgA nephropathy (IgAN), for which the committee has awarded conditional marketing authorization.
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Liver disease

Adverse event halts Inventiva’s pivotal lanifibranor NASH trial

Feb. 16, 2024
By Caroline Richards
Inventiva SA has halted enrollment in its pivotal phase III Nativ3 trial with nonalcoholic steatohepatitis (NASH) candidate lanifibranor after a patient experienced raised liver enzymes indicative of autoimmune hepatitis. The resulting delays to the study could spell trouble for the firm, which estimates its cash runway will only see it through to the start of the third quarter 2024.
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Biogen’s ataxia drug, Crispr’s sickle cell therapy cleared in EU

Feb. 13, 2024
By Caroline Richards
The European Commission approved two therapies for progressive, genetic diseases: Biogen Inc.’s Friedreich’s ataxia drug, Skyclarys (omaveloxolone), and Crispr Therapeutics AG’s CRISPR/Cas9 gene therapy for sickle cell disease and transfusion-dependent beta-thalassemia, Casgevy (exagamglogene autotemcel, exa-cel).
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Sangamo’s early phase I/II Fabry Staar data shine but funds needed for late-stage advancement

Feb. 6, 2024
By Caroline Richards
Sangamo Therapeutics Inc.’s gene therapy for Fabry disease, isaralgagene civaparvovec (ST-920), is continuing to show promising efficacy and safety in the phase I/II study, Staar, but further ahead, the company needs to either attract a partner or secure financing to move to a registrational trial.
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Combined candidiasis fungicidal appears superior to miconazole alone in phase II

Jan. 30, 2024
By Caroline Richards
The topical combination therapy miconazole plus domiphen bromide (MCZ-DB) resolved signs and symptoms of acute vulvovaginal candidiasis (VVC) and eradicated the yeast Candida albicans from vaginal swabs to a greater extent than miconazole (MCZ) alone in a phase II study, according to Hyloris Pharmaceuticals SA and Purna Female Healthcare.
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Cancer cell, dropper, test tubes
Newco news

Actimed continues raising funds to progress improved cancer cachexia asset

Jan. 11, 2024
By Caroline Richards
With a sizeable series B financing well underway, Actimed Therapeutics Ltd. is preparing to advance its compound, S-pindolol benzoate (ACM-001), into a phase IIb/III trial to treat cachexia secondary to colorectal cancer, having also recently completed a £4.75 million (US$5 million) series A extension round.
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NIH-NCI chromosomes telomeres
Cancer

Tessellate Bio draws $8.4M in seed to try alternative synthetic lethality approach

Dec. 14, 2023
By Caroline Richards
With an initial €8 million (US$8.4 million) in seed funding in the bank, Tessellate Bio has emerged from stealth to tackle cancers that rely on the less well explored synthetic lethality mechanism of alternative lengthening of telomeres.
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NIH-NCI chromosomes telomeres
Newco news

Tessellate Bio draws $8.4M in seed to try alternative synthetic lethality approach

Dec. 8, 2023
By Caroline Richards
With an initial €8 million (US$8.4 million) in seed funding in the bank, Tessellate Bio has emerged from stealth to tackle cancers that rely on the less well explored synthetic lethality mechanism of alternative lengthening of telomeres.
Read More
Digital lungs illustration
Newco news

Alveogene secures seed, advances AVG-001 for rare respiratory disease

Dec. 1, 2023
By Caroline Richards
Arriving on the gene therapy scene with an undisclosed seed funding sum, Alveogene is tackling respiratory diseases with high unmet need via a next-generation lentiviral delivery platform to advance into the clinic a candidate for rare inherited disorder alpha-1 antitrypsin deficiency.
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