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Research Report
Comprehensive Report on PF-08046037: An Investigational PD-L1 Targeted TLR7 Agonist Immune-Stimulating Antibody Conjugate
1. Introduction and Overview of PF-08046037
1.1. Identification and Nomenclature
PF-08046037 is an investigational therapeutic agent currently undergoing clinical evaluation. Its primary development code, PF-08046037, is consistently utilized in recent scientific communications and clinical trial registries.[1] The compound was formerly designated SGN-PDL1iT, a nomenclature that indicates its origin and initial development phase by Seagen.[1] Additional synonyms found in various databases include PDL1iT.[2] The consistent cross-referencing of SGN-PDL1iT with PF-08046037 is essential for tracing the molecule's developmental history and acknowledging its technological provenance from Seagen's research pipeline.
1.2. Originator and Current Developer
PF-08046037 was conceived and underwent its initial stages of development at Seagen, Inc., a biotechnology firm recognized for its pioneering work and extensive expertise in the field of antibody-drug conjugate (ADC) technology.[2] Subsequent to Pfizer Inc.'s strategic acquisition of Seagen, PF-08046037 has been integrated into Pfizer's oncology portfolio and is now under active development by Pfizer.[1] This transition is a significant marker of Pfizer's intensified commitment to oncology, particularly through the incorporation of Seagen's advanced ADC and Immune-Stimulating Antibody Conjugate (ISAC) platforms.[4] The acquisition has endowed Pfizer with promising pipeline candidates like PF-08046037 and the specialized expertise crucial for their continued advancement.
1.3. Drug Classification
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/05/16 | Phase 1 | Recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |