On April 4, 2024 ProfoundBio, a clinical-stage biotechnology company dedicated to developing novel antibody-drug conjugate (ADC) therapies for patients with cancer, reported its participation at the upcoming American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2024, taking place from April 5-10 in San Diego, California (Press release, ProfoundBio, APR 4, 2024, View Source [SID1234641795]). ProfoundBio will showcase its innovative ADC programs through an oral presentation on its EGFR- and cMET-dual targeting ADC PRO1286, a poster presentation detailing preclinical data of a SLITRK6-directed ADC PRO1106, and a late-breaking poster presentation on a CD98-directed ADC developed in partnership with Huahui Health, a clinical-stage biotechnology company.
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"We are pleased to share our latest research at the AACR (Free AACR Whitepaper) Meeting this year," stated Zhu Chen, Ph.D., Chief Scientific Officer of ProfoundBio. "These presentations underscore our commitment to leveraging our proprietary ADC platforms to target some of the most challenging cancers. With PRO1286, PRO1106, and our CD98-directed ADC, we are aiming to provide patients with more effective and tolerable treatment options, and look forward to sharing the latest findings with the scientific community."
Key Presentations at AACR (Free AACR Whitepaper) 2024
Abstract #
Presentation Title
Date/Time
Session Track
Presenter(s)
2050
Preclinical characterization
of PRO1106, a novel and
promising SLITRK6-directed
sesutecan ADC
April 8,
2024,
9:00 AM –
12:30 PM
Poster Session,
Experimental and
Molecular
Therapeutics
Zhu Chen,
ProfoundBio
6580
A novel EGFR x cMET
bispecific ADC PRO1286
demonstrated broad
antitumor activity and
promising tolerability in
preclinical models
April 9,
2024,
3:05 PM –
3:20 PM
Minisymposium,
Experimental and
Molecular
Therapeutics,
Chemistry
Zhu Chen,
ProfoundBio
LB425
A tumor microenvironment –
targeting CD98-directed ADC
confers robust anti-tumor
activity in multiple cancers
with favorable
pharmacokinetics and safety
profiles in preclinical models
April 10,
2024,
9:00 AM –
12:30 PM
Late-Breaking
Poster Session,
Experimental and
Molecular
Therapeutics
Bin Chen,
Huahui Health
Zhu Chen,
ProfoundBio
About ProfoundBio’s ADC Programs
FRα-Targeted ADC: Rinatabart sesutecan (Rina-S, PRO1184)
Rina-S is a FRα-targeted ADC being developed as a novel treatment option for patients with ovarian and endometrial cancer, and other FRα-expressing cancers. Rina-S is comprised of a FRα-directed antibody conjugated to sesutecan, ProfoundBio’s novel, proprietary hydrophilic exatecan-based linker-drug, at a homogeneous drug-to-antibody ratio (DAR) of 8. Exatecan is a potent, membrane permeable topoisomerase-1 inhibitor with strong bystander effect. The linker component of sesutecan is a highly hydrophilic, stable, cleavable linker designed to mask the hydrophobicity of exatecan, enabling high DAR and efficient delivery of the exatecan payload to tumors while maintaining favorable physicochemical and pharmacokinetic properties of the ADC. Rina-S is currently being evaluated in a Phase 1/2 clinical trial (NCT05579366) and has been granted Fast Track Designation by the U.S. Food and Drug Administration (FDA) for the treatment of patients with FRα-expressing high-grade serous or endometrioid platinum-resistant ovarian cancer.
CD70-Targeted ADC: PRO1160
PRO1160 is an ADC consisting of a CD70-targeted antibody conjugated to ProfoundBio’s novel, proprietary hydrophilic exatecan-based linker-drug, sesutecan. CD70 is a protein expressed on both solid tumors and hematological malignancies including renal cell carcinoma, nasopharyngeal carcinoma, and non-Hodgkin lymphoma, yet is largely absent in normal tissues. With preclinical results showcasing encouraging pharmacokinetics, efficacy, and tolerability, PRO1160 is emerging as a potential advancement in the treatment of these cancers and is currently being evaluated in a Phase 1/2 clinical trial (NCT05721222).
PTK7-Targeted ADC: PRO1107
PRO1107 is an ADC consisting of a PTK7-targeted antibody conjugated to ProfoundBio’s novel, proprietary hydrophilic MMAE-based linker-drug, LD343, at a homogeneous DAR of 8. MMAE is a potent, membrane-permeable microtubule inhibitor that has been clinically validated as an ADC payload with multiple marketed vedotin ADCs at a DAR of 4. The linker component of LD343 is a highly hydrophilic, stable, cleavable linker designed to mask the hydrophobicity of MMAE, enabling high DAR and efficient delivery of the MMAE payload to tumors while maintaining favorable physicochemical and pharmacokinetic properties of the ADC. PRO1107 is currently being evaluated in a Phase 1/2 clinical trial (NCT06171789).
Bispecific ADC: PRO1286
PRO1286 is a novel EGFR- and cMET-dual targeting ADC that has the potential to treat a broad range of tumors. PRO1286 is built on the clinically validated sesutecan platform and is anticipated to enter the clinic in 2024.