Shifting Medicine Forward

Our path toward disease-centric therapies

ONCOLOGY
Ichnos continues to advance its pipeline of multispecific antibodies in oncology, with lead asset ISB 1342 in Phase 1, and ISB 1442 in IND-enabling studies. Please contact us at corporate.communications@ichnossciences.com if you are interested in exploring a partnership.
Asset Description Preclinical Phase 1 Phase 2 Phase 3 Status

Products
ISB 1342
CD38 x CD3 BEAT® 1.0 bispecific antibody
Relapsed/Refractory Multiple Myeloma (R/R MM); T-ALL under consideration
      Phase 1 Enrolling
ISB 1442
CD38 x CD47 BEAT® 2.0 bispecific antibody
R/R MM; AML and T-ALL under consideration
      PHASE 1 INITIATION
ISB 2001
BCMA x CD38 x CD3 TREAT™ trispecific antibody
R/R MM
      IND-Enabling Studies

Candidates
ISB 2004
BEAT® 2.0 bispecific antibody
Hematologic Malignancies/ Solid Tumors
      Discovery
ISB 2005
TREAT™ trispecific antibody
Solid Tumors
      Discovery

Products

Compound:
ISB 1342
Target:
CD38 x CD3 BEAT® 1.0 bispecific antibody
Indication:
Relapsed/Refractory Multiple Myeloma (R/R MM); T-ALL under consideration
Phase:
phase-1
Status:
Phase 1 Enrolling
Compound:
ISB 1442
Target:
CD38 x CD47 BEAT® 2.0 bispecific antibody
Indication:
R/R MM; AML and T-ALL under consideration
Phase:
phase-1
Status:
PHASE 1 INITIATION
Compound:
ISB 2001
Target:
BCMA x CD38 x CD3 TREAT™ trispecific antibody
Indication:
R/R MM
Phase:
preclinical
Status:
IND-Enabling Studies

Candidates

Compound:
ISB 2004
Target:
BEAT® 2.0 bispecific antibody
Indication:
Hematologic Malignancies/ Solid Tumors
Phase:
preclinical
Status:
Discovery
Compound:
ISB 2005
Target:
TREAT™ trispecific antibody
Indication:
Solid Tumors
Phase:
preclinical
Status:
Discovery


BEAT®: Bispecific Engagement by Antibodies based on the TCR
TREAT™: Trispecific Engagement by Antibodies based on the TCR

 
Autoimmune Disease
Ichnos is out-licensing its autoimmune disease assets to enable greater focus on oncology. Explore the pipeline chart below to learn more and contact us at Corporate.Communications@ichnossciences.com for additional information.
Products Description Preclinical Phase 1 Phase 2 Phase 3 Status
ISB 830 (telazorlimab) (Licensing discussions ongoing)
OX40 antagonist monoclonal antibody
Atopic Dermatitis (AD)*
      Phase 2b completed†
ISB 880 (Licensed to Almirall S.A.)
IL-1RAP antagonist monoclonal antibody
Autoimmune Disease
      IND-Enabling Studies Completed
Autoimmune Disease
Compound:
ISB 830 (telazorlimab) (Licensing discussions ongoing)
Target:
OX40 antagonist monoclonal antibody
Indication:
Atopic Dermatitis (AD)*
Phase:
phase-2
Status:
Phase 2b completed†
Compound:
ISB 880 (Licensed to Almirall S.A.)
Target:
IL-1RAP antagonist monoclonal antibody
Indication:
Autoimmune Disease
Phase:
preclinical
Status:
IND-Enabling Studies Completed
 

*A US IND for rheumatoid arthritis and other autoimmune indications is active.
†Primary efficacy endpoint (EASI score, % change, baseline to week 16) met at two highest doses tested. Numerical improvements were seen for the two higher-dose arms (300 mg and 600 mg q 2 weeks) of telazorlimab compared to placebo in the secondary endpoints of EASI-75 and Investigator Global Assessment, but the differences were generally not statistically significantly different from placebo.

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Career Opportunities

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