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Hansoh initiates the trial of anti-B7H4 ADC plus anti-PD-L1 or anti-VEGF mAbs in solid tumors

Hansoh conducted a new clinical study to evaluate the efficacy of anti-B7H4 ADC in combination with anti-PD-L1 or anti-VEGF mAbs for treating solid tumors. This marks the 3rd clinical trial for HS-20089 in China.

HS-20089 is a novel B7-H4 targeted ADC with a TOPOi payload (DAR=6), developed by Hansoh and licensed to GSK with an $85 million upfront payment.

Factors controlling B7-H4 and B7-H4 receptor expression
Factors controlling B7-H4 and B7-H4 receptor expression

The clinical study

This study contains four combination therapy cohorts, each consisting of a dose exploration part and a dose expansion part.

The combination includes Adebrelimab, an anti-PD-L1 monoclonal antibody, either with or without platinum, or Bevacizumab with or without platinum. Adebrelimab was an anti-PD-L1 monoclonal antibody discovered and launched by Hengrui in China as their second anti-PD-(L)1 therapy.

The clinical trial identified as NCT06336707 is expected to enroll a total of 1,048 participants, while the trial registered in China (CTR20241023) showed an enrollment of 208 patients.

Anti-B7H4 ADC

Product

Company

Combo

Stage

Enrollment

Initiation

AZD8205

AstraZeneca

-

Phase 1/2

248

2021.10.18

HS-20089

Hansoh/GSK

-

Phase 1

177

2022.01.05

-

Phase 2

460

2023.12.31

Adebrelimab

Bevacizumab

Phase 1

1,048

2024.04.08

SGN-B7H4V

Seagen/Pfizer

-

Phase 1

430

2022.01.12

XMT-1660

Mersana

-

Phase 1

319

2022.08.15

BG-C9074

Beigene

Tislelizumab

Phase 1

150

2024.05.06

Last month, we reported that Beigene commenced the first-in-human trial (NCT06233942) of BG-C9074 mono or in combination with  anti-PD-1 mAb. BG-C9074 is an ADC that targets B7-H4. It has a DAR of 6 and was developed in collaboration with DualityBio.

Mersana has announced that the XMT-1660 trial's dose escalation phase is currently underway, with an escalated dose of 59 mg/m2. The Maximum Tolerated Dose (MTD) has not yet been determined. Furthermore, they are also enrolling patients in backfill cohorts to optimize the dosage and schedule.

AZD8205 has moved from phase 1 to phase 2 as of 2022 Q2. The results are expected to be available in 2025.

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