Biocon Biologics acquires biosimilars business of Viatris for $3bn

30 November | DEALS

Biocon subsidiary Biocon Biologics has acquired the international biosimilars business of Viatris in a deal totalling $3bn. In February, the companies signed a definitive agreement for the acquisition, which would aid Biocon Biologics in establishing a completely integrated international biosimilars enterprise, with eight products currently in the market.

Under the deal, Viatris received an upfront payment of $2bn from Biocon Biologics, which also issued compulsorily convertible preference shares (CCPS) worth $1bn in the company.  This CCPS is equal to an equity stake of a minimum of 12.9% on a fully diluted basis. With the takeover, Biocon Biologics now has complete ownership of its partnership assets, namely bTrastuzumab, bPegfilgrastim, bBevacizumab, bGlargine, bAspart, bPertuzumab and bGlargine 300U. The company also received rights from Viatris for bAdalimumab and bEtanercept, which are in-licenced immunology products. Additionally, Viatris’ rights for bAflibercept were obtained by Biocon Biologics. This therapy is intended for the treatment of various ophthalmology conditions.

16 November | DEALS

Jnana partners with Roche to discover drugs for multiple targets

Jnana Therapeutics and Roche have signed a second partnership and licence agreement to discover small-molecule drugs to treat cancer, immune-mediated and neurological ailments. The deal covers multiple targets from a varying range of target classes for addressing ailments with high unmet needs.

For discovering new small molecule drugs against various disease targets, Jnana will leverage its RAPID chemoproteomics platform. According to the partnership, Roche will make $50m in upfront payments to Jnana. Jnana is also entitled to receive substantial near-term milestone payments and additional potential payments of more than $2bn in the future, apart from tiered royalty payments.

18 November | DEALS

Regeneron and CytomX partner to develop bispecific cancer therapies

Regeneron Pharmaceuticals has entered a collaboration and licensing agreement with CytomX Therapeutics for developing conditionally-activated bispecific cancer therapies. Under the deal, the companies will work together on the discovery activities for identifying and validating the conditionally active bispecific antibodies.

This collaboration will use Regeneron ’s Veloci-Bi bispecific antibody development platform and CytomX’s Probody therapeutic platform. It will focus on applying CytomX’s biologic masking strategies for developing the investigational Regeneron bispecific cancer therapies, which are activated by proteases in the tumour microenvironment. According to the agreement, CytomX will receive a $30m upfront payment and is eligible to receive up to $2bn in preclinical, clinical, and commercial milestones.

7 December | DEALS

GSK, Sanofi, Takeda and scientists in Singapore partner for biologics

GSK, Sanofi and Takeda are set to collaborate with researchers from the Agency for Science, Technology and Research (A*STAR), National University of Singapore (NUS), Nanyang Technological University , Singapore (NTU Singapore), NTUitive and Singapore Institute of Technology (SIT) to boost biologics and vaccine manufacturing expertise in the country.

This collaboration will be validated through the consortium, Biologics Pharma Innovation Programme Singapore (BioPIPS), initiated by A*STAR with the Singapore Economic Development Board’s (EDB) support.

BioPIPS plans to utilise research and innovation to enhance the biologics manufacturing expertise of Singapore, which comprises recombinant therapeutic proteins and vaccines. Additionally, BioPIPS intends to equip the country’s biologics production expertise for launching new products and manufacturing technologies.

28 November | R&D

UK Government to fund research into new obesity treatments

The UK Government has announced funds worth $24.17m (£20m) to conduct research for developing new obesity therapies and technologies. These therapies and digital tools have been demonstrated to aid people in shedding 20% of their weight. Every year, obesity costs a staggering $7.2bn (£6bn) to the UK National Health Service (NHS), and by 2050, the figure is expected to increase to more than $11.7bn (£9.7bn) per year.

To detect sites for this research, which will analyse how new and possibly transformative therapies can be merged with technologies such as digital tools to boost durable health outcomes in obese patients, an open competition will be run early next year. 

1 December | FUNDING

UTMB and HDT Bio receive US funding for vaccine development

The University of Texas Medical Branch (UTMB) and HDT Bio  have received funding worth up to $87.4m in a project agreement from the US Government for developing self-amplifying RNA (saRNA) vaccine technology against advanced and emergent viral threats.

The award is provided by Joint Program Executive Office for Chemical, Biological, Radiological, and Nuclear Defense (JPEO-CBRND) of the US Department of Defense (Dod ) and the Biomedical Advanced Research and Development Authority (BARDA) of the US Department of Health and Human Services (HHS), through the Medical CBRN Defense Consortium (MCDC) Other Transaction Authority (OTA).

In Brief

Kite and Daiichi Sankyo update cell therapy licensing agreement

Kite Pharma and Daiichi Sankyo have updated a partnership agreement signed in 2017 for the former’s CAR T-cell therapy, Yescarta (axicabtagene ciloleucel).  Under the prior deal, Daiichi Sankyo acquired exclusive rights for the development, manufacturing and commercialisation of Yescarta in Japan.

Touchlight and Odimma enter cancer therapy clinical material supply agreement

Touchlight and Odimma Therapeutics have entered an agreement for the development and supply of clinical material for usage in the latter’s neoantigen programme for cancer. The programme is anticipated to commence clinical enrolment next year.

MEI and Kyowa Kirin to discontinue development of zandelisib outside Japan

MEI Pharma and Kyowa Kirin have announced plans to discontinue the international development of investigational cancer therapy, zandelisib, for B-cell malignancies outside of Japan. The latest development comes after the companies received guidance from a meeting held with the US FDA in November.

Sanofi and Queensland collaborate to build $190m research facility

Sanofi has signed an agreement with the Queensland Government in Australia to establish a $190m (A$280m) research facility in Brisbane. According to the latest deal, the University of Queensland (UQ) and Griffith University will serve as foundational partners.

24 November | R&D

Biovac and IVI enter deal to develop oral cholera vaccine

South African bio-pharmaceutical firm BIOVAC and the International Vaccine Institute (IVI) in South Korea have signed a licencing and technology transfer agreement for developing and manufacturing an oral cholera vaccine (OCV).

The deal will aid Biovac in establishing drug substance manufacturing expertise for producing the antigen/raw material required to make the vaccines.

This collaboration with IVI will enable Biovac to licence and transfer technology to boost manufacturing volumes, which in turn cuts down the crucial shortage of cholera vaccines across the globe. The initial segment of the project is supported by $6.9m (R120m) funds from Wellcome Trust and the Bill & Melinda Gates Foundation.

1 December | DEALS

Liminatus Pharma enters SPAC merger deal with Iris Acquisition

Liminatus Pharma has entered a definitive business combination agreement with special purpose acquisition company (SPAC) Iris Acquisition to create a business with a pro forma enterprise value of nearly $334m. 

The new entity is anticipated to receive up to $316m in gross cash proceeds. This includes $276m held in the trust account of Iris and equity private investment in public equity (PIPE) funding of $15m and convertible note financing worth $25m. A clinical-stage biopharmaceutical firm, Liminatus focuses on the development of new therapies for cancer that utilises the immune system of the body to detect and fight cancer cells. 

In brief

Kite and Daiichi Sankyo update cell therapy licensing agreement

Kite Pharma and Daiichi Sankyo have updated a partnership agreement signed in 2017 for the former’s CAR T-cell therapy, Yescarta (axicabtagene ciloleucel).  Under the prior deal, Daiichi Sankyo acquired exclusive rights for the development, manufacturing and commercialisation of Yescarta in Japan.

Touchlight and Odimma enter cancer therapy clinical material supply agreement

Touchlight and Odimma Therapeutics have entered an agreement for the development and supply of clinical material for usage in the latter’s neoantigen programme for cancer. The programme is anticipated to commence clinical enrolment next year.

MEI and Kyowa Kirin to discontinue development of zandelisib outside Japan

MEI Pharma and Kyowa Kirin have announced plans to discontinue the international development of investigational cancer therapy, zandelisib, for B-cell malignancies outside of Japan. The latest development comes after the companies received guidance from a meeting held with the US FDA in November.

Sanofi and Queensland collaborate to build $190m research facility

Sanofi has signed an agreement with the Queensland Government in Australia to establish a $190m (A$280m) research facility in Brisbane. According to the latest deal, the University of Queensland (UQ) and Griffith University will serve as foundational partners.