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BioWorld - Tuesday, June 2, 2026
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

Tibia, fibula, femor and knee illustration

Novadip raises $22M in series B funding for US trial of bone regeneration therapy

Oct. 28, 2021
By Cormac Sheridan
DUBLIN – Novadip SA raised €19 million (US$22.1 million) in a first close of a series B round to progress its autologous bone regeneration therapy, NVD-003, on either side of the Atlantic. The company is also working on an allogeneic regenerative approach, which is still preclinical.
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Oncopeptides stock craters as it pulls multiple myeloma drug Pepaxto from U.S. market

Oct. 22, 2021
By Cormac Sheridan
DUBLIN – Oncopeptides AB has withdrawn its troubled multiple myeloma drug Pepaxto (melphalan flufenamide) from the U.S. market, less than eight months after receiving an accelerated approval from the FDA. The move comes less than a week before the FDA’s Oncologic Drugs Advisory Committee was due to consider the drug’s safety profile because of data anomalies that surfaced over the summer.
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European Union flag, coins

Sofinnova Partners ‘blasted through its target’ with $550M for 10th early stage fund

Oct. 19, 2021
By Cormac Sheridan
DUBLIN – Sofinnova Partners closed out its flagship Capital X fund at €472 million (US$550 million), providing further evidence that private equity investing in European biotechnology and medical technology remains in rude health. It represents, managing partner Graziano Seghezzi told BioWorld, one of the most successful fundraising campaigns in its 30-year history. “We went out and raised this fund in six months.”
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South Korean flag on building

D&D Pharmatech closes $51M series C round, eyes Seoul IPO

Oct. 19, 2021
By Cormac Sheridan
D&D Pharmatech Inc., a Korean-American firm commercializing innovation from Johns Hopkins University raised $51 million in a pre-IPO series C round, which sets the stage for an IPO in Seoul early next year.
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siRNA bound to mRNA

Silence reaches China with siRNA deal worth up to $1.3B

Oct. 19, 2021
By Cormac Sheridan
DUBLIN – Silence Therapeutics plc has entered the Chinese market through a partnering deal with Hansoh Pharmaceutical Group Co. Ltd. that involves developing short interfering RNA (siRNA) drugs against three undisclosed targets. The London-based firm is getting $16 million up front and could earn as much as $1.3 billion in development, regulatory and commercial milestones across the alliance. It will also receive tiered sales royalties, ranging from low double digits to mid-teens in percentage terms.
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siRNA bound to mRNA

Silence reaches China with siRNA deal worth up to $1.3B

Oct. 15, 2021
By Cormac Sheridan
DUBLIN – Silence Therapeutics plc has entered the Chinese market through a partnering deal with Hansoh Pharmaceutical Group Co. Ltd. that involves developing short interfering RNA (siRNA) drugs against three undisclosed targets.
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Coins and charts

Tentarix closes $50M series A round to probe ‘combinatorial space’ for multifunctional drugs

Oct. 14, 2021
By Cormac Sheridan
Tentarix Biotherapeutics LP broke cover with $50 million in series A funding to take forward an industrialized flow cytometry platform that enables it to screen rapidly for multifunctional antibody-based drugs.
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Abalos adds $38M in series A extension to take virotherapy into the clinic

Oct. 14, 2021
By Cormac Sheridan
DUBLIN – Abalos Therapeutics GmbH raised €32.5 million (US$37.6 million) in a series A extension, taking the total raise to €43 million, enough to enable the company to generate clinical proof-of-concept data with its lead viral immunotherapy for cancer.
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Epilepsy gene therapy deal ‘Sparks’ 172% stock surge at Combigene

Oct. 12, 2021
By Cormac Sheridan
Dublin – Shares in Combigene AB, a little-known Swedish gene therapy firm, surged upward by 172% Oct. 12 on news of a preclinical licensing deal in epilepsy with Spark Therapeutics, which is potentially worth $328.5 million.
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Idorsia stock clipped by phase III miss in Fabry disease

Oct. 12, 2021
By Cormac Sheridan
DUBLIN – Shares in Idorsia Ltd. were off almost 4% Oct. 11 on news that lucerastat missed the primary endpoint of the Modify phase III trial in Fabry disease. The double-blinded, placebo-controlled study, which recruited 118 adult patients, was designed to evaluate the effect of lucerastat on neuropathic pain. Patients were randomized to drug or placebo in a 2-to-1 ratio.
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