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BioWorld - Saturday, May 30, 2026
Home » Topics » Asia-Pacific » Australia

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Mesoblast raises AU$75M to prepare for U.S. launch of allogeneic cell therapy

Oct. 4, 2019
By Tamra Sami
PERTH, Australia – Australian cell therapy developer Mesoblast Ltd. has completed a AU$75 million (US$50.32 million) capital raising via an oversubscribed placement to existing and new Australian and global institutional investors.
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Australia may allow more self-test IVDs to be sold to consumers

Oct. 3, 2019
By Tamra Sami
PERTH, Australia – Australia's Therapeutic Goods Administration (TGA) is seeking comments from stakeholders on whether certain self-testing in vitro diagnostics (IVDs) should be prohibited from being sold to consumers.
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Australian government urged to provide immunotherapy access for high-risk melanoma patients

Oct. 2, 2019
By Tamra Sami
PERTH, Australia – Australia is at risk of falling behind the U.S. and Europe in preventing recurrence of melanoma, the Melanoma Institute Australia warns. It is urging the Australian government to undertake a timely review of immunotherapy treatments effective in preventing the spread of melanoma and to fast track listings on the government-subsidized Pharmaceutical Benefits Scheme (PBS).
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Fujifilm licenses Cynata's stem cell therapy for GVHD in deal worth $43M+

Sep. 25, 2019
By Tamra Sami
PERTH, Australia – Melbourne-based regenerative medicine company Cynata Therapeutics Ltd. is enjoying a bit of hot pursuit as Fujifilm Corp. exercised its license option to develop and commercialize Cynata's lead Cymerus mesenchymal stem cell (MSC) product, CYP-001, for graft-vs.-host disease (GVHD) at the same time that Cynata is an acquisition target by Dainippon Sumitomo.
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Saluda Medical gains EU approval for Evoke SCS device for chronic pain

Sep. 19, 2019
By Tamra Sami

FDA grants IDE approval for pivotal study of Avita Medical's Recell system

Sep. 18, 2019
By Liz Hollis
Melbourne, Australia-based regenerative medicine company Avita Medical Ltd. has received good news from the FDA. The company, which also has a presence in Valencia, Calif., said the agency gave its thumbs up to an investigational device exemption application for a pivotal trial (NCT04091672) evaluating the safety and effectiveness of the Recell autologous cell harvesting device in combination with meshed autografting for the treatment of acute full-thickness skin defects, such as degloving, crush wounds, abrasions, lacerations and surgical wounds.
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Australia proposes revising device essential principles to align with international practices

Sep. 17, 2019
By Tamra Sami
PERTH, Australia – The Therapeutic Goods Administration (TGA) is seeking feedback on a proposal that to change Australia's medical device essential principles for safety and performance to more closely mirror the new EU Medical Device Regulation (EU MDR).
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Australia's Mesoblast inks potential $1B deal with Germany's Grünenthal

Sep. 11, 2019
By Tamra Sami
PERTH, Australia – Australian cell therapy developer Mesoblast Ltd. has partnered with Germany's Grünenthal Group to develop and commercialize Mesoblast's allogeneic cell therapy candidate, MPC-06-ID, in a deal that carves out Europe, Latin America and the Caribbean.
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Exopharm enters clinic with exosome therapy that could disrupt stem cell therapies

Sep. 11, 2019
By Tamra Sami
PERTH, Australia – Stem cell therapy has failed to deliver on its promises, according to Exopharm Ltd. founder and CEO Ian Dixon, who said he believes that exosomes, or the extracellular vesicles released by stem cells, could be a disrupter in the regenerative medicine space.
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Exopharm enters clinic with exosome therapy that could disrupt stem cell therapies

Sep. 9, 2019
By Tamra Sami
PERTH, Australia – Stem cell therapy has failed to deliver on its promises, according to Exopharm Ltd. founder and CEO Ian Dixon, who said he believes that exosomes, or the extracellular vesicles released by stem cells, could be a disrupter in the regenerative medicine space.
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