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Theratechnologies Inc T.TH

Alternate Symbol(s):  THTX

Theratechnologies Inc. is a Canada-based clinical-stage biopharmaceutical company. The Company is focused on the development and commercialization of therapies addressing unmet medical needs. It markets prescription products for people with human immunodeficiency viruses (HIV) in the United States. The Company's research pipeline focuses on specialized therapies addressing unmet medical needs in HIV, nonalcoholic steatohepatitis (NASH) and oncology. Its medicines include Trogarzo and EGRIFTA SV (tesamorelin for injection). Trogarzo (ibalizumab-uiyk) injection is a long-acting monoclonal antibody which binds to domain 2 of the CD4 T cell receptors. EGRIFTA SV (tesamorelin for injection) is approved in the United States for the reduction of excess abdominal fat in people with HIV who have lipodystrophy. Its portfolio includes Phase I clinical trial of sudocetaxel zendusortide (TH1902), a novel peptide-drug conjugate (PDC), in patients with advanced ovarian cancer.


TSX:TH - Post by User

Comment by qwerty22on Oct 04, 2021 2:23pm
113 Views
Post# 33961675

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:My opinion

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:My opinionOn a brighter note. Cancer deal.

"With a re­cent ap­proval for lung can­cer bis­pe­cif­ic ami­van­tam­ab, J&J is look­ing to build a fran­chise in that space with a grow­ing crop of drugs in the pipeline. The drug gi­ant has now tapped a fa­mil­iar part­ner to dri­ve that work ahead, and the pair is go­ing af­ter a well-known tar­get.

J&J's Janssen unit has inked a li­cens­ing deal worth $100 mil­lion in up­front cash and $25 mil­lion in eq­ui­ty for glob­al li­cens­ing rights to Xen­cor's CD20/CD3 bis­pe­cif­ic an­ti­body plam­o­tam­ab cur­rent­ly in Phase I test­ing against B cell ma­lig­nan­cies, the com­pa­nies said Mon­day.

The deal will come with up to $1.18 bil­lion in down­stream mile­stones as well as po­ten­tial roy­al­ties in the "mid-teens to low twen­ties," ac­cord­ing to a re­lease.

Janssen will hold ex­clu­sive de­vel­op­ment and com­mer­cial­iza­tion rights world­wide for plam­o­tam­ab, in­clud­ing in monother­a­py and com­bo reg­i­mens, with Xen­cor and Janssen split­ting fu­ture clin­i­cal tri­al costs 20-80, re­spec­tive­ly. Those plans in­clude a sub­cu­ta­neous for­mu­la­tion tri­al for the bis­pe­cif­ic, which is ex­pect­ed to be­gin in 2022. Mean­while, Xen­cor will ex­clu­sive­ly fund a Phase II com­bo study of plam­o­tam­ab, taf­a­sita­m­ab and lenalido­mide in pa­tients with B-cell lym­phoma set to start in late 2021 or ear­ly 2022.

The col­lab­o­ra­tion will al­so fu­el R&D for new CD28-tar­get­ing bis­pecifics out of Xen­cor's pipeline, with the part­ners col­lab­o­rat­ing on a two-year re­search project. Janssen will hold an ex­clu­sive world­wide li­cense to de­vel­op any se­lect­ed mol­e­cules that come out of that work as part of a com­bo with plam­o­tam­ab or oth­er an­ti­bod­ies, in­clud­ing those tar­get­ing CD3, where they would com­pete di­rect­ly with Re­gen­eron."

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