TRANSCENTA HOLDING - A Global Fully Integrated Biotherapeutics Company

Transcenta, Biologics, Antibody, Claudin 18.2

TRANSCENTA HOLDING - A Global Fully Integrated Biotherapeutics Company

Careers Contact

Pipeline

Transcenta is developing a diverse pipeline of more than a dozen novel biologic therapies for oncology and selected non-oncology indications including bone and kidney disorders.

Oncology pipeline includes multiple innovative and differentiated biologic molecules targeting major cancer pathways which have potential synergistic mechanisms of actions for tumor indications with high unmet medical needs. Our pipeline includes both targeted therapy Osemitamab (TST001) as well as immunotherapy (TST005) that engage either NK cells or T cells to kill tumor cells, or agents that can enhance the anti-tumor activity of the above mentioned therapies by either inhibiting tumor associated fibroblast derived immunosuppressive regulatory protein (TST003) or depleting immunosuppressive Treg cells (TST010) or by enhancing TIL infiltration into the tumor by normalizing vasculature (MSB0254).

Transcenta’s highly differentiated non-oncology pipelines focus on novel indications with high unmet medical needs in bone and kidney diseases. TST002 and TST004 are two differentiated molecules that are designed to treat osteoporosis and complement mediated disease respectively. Both osteoporosis and kidney disease like IgAN are areas of high unmet medical needs and with high market potentials.
Oncology
Drugs
Candidate
Target
Indication
Modality
Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Rights
Partner
Osemitamab (TST001)
Claudin 18.2
G/GEJC and Other Solid Tumors
G/GEJC and Other Solid Tumors
mAb
Osemitamab (TST001)
More + More +

Drugs Candidate:Claudin 18.2

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
G/GEJC and Other Solid Tumors -mAb - Combo with PL1/Chemo
Combo with PL1/Chemo
G/GEJC and Other Solid Tumors - - Combo with Chemo
Combo with Chemo
Global
In-house
READ MORE READ MORE
TST106
Claudin 18.2-X
G/ GEJC and other Solid Tumors
BsADC

Drugs Candidate:Claudin 18.2-X

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
G/ GEJC and other Solid Tumors -BsADC - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST198
Claudin 18.2
G/ GEJC and other Solid Tumors
RDC

Drugs Candidate:Claudin 18.2

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
G/ GEJC and other Solid Tumors -RDC - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST003
Gremlin-1
Colorectal and Prostate Cancers
mAb

Drugs Candidate:Gremlin-1

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Colorectal and Prostate Cancers -mAb - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST786
PD1-VEGF and Gremlin-1
Colorectal and Prostate Cancers
TsAbs

Drugs Candidate:PD1-VEGF and Gremlin-1

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Colorectal and Prostate Cancers -TsAbs - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST005
PD-L1 x TGF-β
Solid Tumors
BsAb

Drugs Candidate:PD-L1 x TGF-β

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Solid Tumors -BsAb - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST013
LIV-1
Solid Tumors
ADC

Drugs Candidate:LIV-1

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Solid Tumors -ADC - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST105
FGFR2b-X
Solid tumors
BsADC

Drugs Candidate:FGFR2b-X

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Solid tumors -BsADC - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
Ozekibart
DR5
Chondrosarcoma
Agonist Antibody
Ozekibart
More + More +

Drugs Candidate:DR5

Right:Greater China

Partner:Inhibrx

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Chondrosarcoma -Agonist Antibody - Monotherapy
Monotherapy
Greater China
Inhibrx
READ MORE READ MORE
Non-oncology
Drugs
Candidate
Target
Indication
Modality
Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Rights
Partner
Blosozumab (TST002)
Sclerostin
Osteoporosis
mAb
Blosozumab (TST002)
More + More +

Drugs Candidate:Sclerostin

Right:Greater China

Partner:In-licensed from Eli Lilly

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Osteoporosis -mAb - Monotherapy
Monotherapy
Greater China
In-licensed from Eli Lilly
READ MORE READ MORE
TST004
MASP-2
IgAN, TMA
mAb

Drugs Candidate:MASP-2

Right:Global

Partner:Co-development with Alebund in Greater China

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
IgAN, TMA -mAb - Monotherapy
Monotherapy
Global
Co-development with Alebund in Greater China
READ MORE READ MORE
TST801
BAFF/APRIL
Autoimmune Disease
BsP

Drugs Candidate:BAFF/APRIL

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
Autoimmune Disease -BsP - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST808
APRIL
IgAN
HLE BpAb

Drugs Candidate:APRIL

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
IgAN -HLE BpAb - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TST008
BAFF/MSAP-2
IgAN
BsAb

Drugs Candidate:BAFF/MSAP-2

Right:Global

Partner:In-house

Preclinical
IND
Phase I
Phase II
Pivotal Phase III
IgAN -BsAb - Monotherapy
Monotherapy
Global
In-house
READ MORE READ MORE
TOP
肿瘤

MSB2311*

靶点:PD-L1

适应症:TMB-H 实体瘤

模态:中国

权利:全球

合伙人:内部

MSB2311 是靶向结合 PD-L1 的研究性 pH 依赖性人源化抗体。

PD-L1 参与抑制了对抗癌症的免疫系统应答,在实体瘤患者的肿瘤细胞中PD-L1表达水平显著升高。MSB2311 使用了工程改造去除了和Fc受体结合的人源IgG1。MSB2311 可与肿瘤细胞上的 PD-L1 结合,并阻断 PD-L1 和 PD-1(T效应细胞上的受体)的相互作用。此外,MSB2311 与 PD-L1 的结合引发 MSB2311 的内吞,当进入 pH 值低于5.5 的核内体时,MSB2311 可从结合的 PD-L1 上分离, MSB2311 可在 FcRn 的帮助下再循环到质膜,并重新与其他肿瘤细胞上的 PD-L1 结合。临床前研究结果表明,MSB2311 在同源小鼠模型中可抑制有表达 PD-L1 的肿瘤细胞的肿瘤生长。