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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

Post by Wino115on Dec 07, 2021 2:00pm
340 Views
Post# 34207245

Trodelvy's most direct competitor in TNBC Ph 1 data released

Trodelvy's most direct competitor in TNBC Ph 1 data released

Here’s some Phase 1 results from the drug most see as the nearest direct competitor in TNBC to Trodelvy at this point (because TH1902 is not very well known!).  It’s from Daiichi Sankyo and Astra Zeneca and called DS-1062.

 

Data is from cutoff of Jul30 and for 44 TNBC patient cohort of the TROPION study.  Recall it’s a Topo1 inhibitor ADC.

 

 —-Objective Response Rate was 32% — in line with Trodelvy

 —- Disease Control Rate was 77% (disease control is total of complete, partial and stable disease).

 —- In TOPO-1 ADC Naive subset, ORR was 48%  —better than Trodelvy in apples-to-apples cohort

 —- Baseline had 11% with brain metastases, 68% 2 prior lines, 30% treated with TOPO-1 ADCs

 —- Disease Control “observed” beyond 7 months in patients with ongoing response

 —- No median Duration of Response reached at current date cutoff

 

Safety Summary:

 —-Grade 3 or higher TEAE’s in 23% (TEAE = Treatment Emergent Adverse Event)

 —- Serious treatment related TEAE’s in 5%

 —- Common ones of nausea, stomatitis in 50-60%

 

So seems the hurdle to beat is still around 35% ORR or maybe 50% ORR for those with high sortilin expression (so it’s proper cohort) and having a disease control rate that’s pretty high —so at least a bunch of stables and some partial and complete responses of 50% or hugher. 

 

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