ADC TOXICITY ATLAS
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JK-06

Investigational
JK06; JK 06
Sponsor
Salubris Biotherapeutics
Indication
Unresectable locally advanced / metastatic solid tumors (lead: squamous NSCLC; also breast cancer, basket)
Target family
Other
RP2D dose
4.5 mg/kg
Q3WRP2D
01
Multi-organ toxicity

Fingerprint & organ drill-down

Also reported
0%severity100%
0
Assessed · clear
true 0%
No data
never assessed
2 adverse-event terms

Ocular

Any-grade
10%
G3+
2%
RP2D
sagittal schematic · Unknown

Tissues shaded by reported adverse-event rate.

Cornea
AE
-
Express.
-
Limbus
AE
-
Express.
-
Conjunctiva
AE
-
Express.
-
Lens
AE
-
Express.
-
Retina / RPE
AE
-
Express.
-
Dominant tissue
Cornea
Surface subtype
Corneal (off-target)
Reversibility
Unknown
Reported ocular events
Dry eye10%
Keratitis-
G3+ 2%n=2
02
Construct

Molecular anatomy

Antibody
Humanized
Linker
2
DAR
Payload
Tubulin inhibitor
Linker structure
structure not applicable
Payload structureC39H67N5O7
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@@H]([C@@H](C)C(=O)N[C@H](C)[C@H](C2=CC=CC=C2)O)OC)OC)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)NC
03
Antibody

Antibody & Fc engineering

Antibody
-
Isotype
-
Origin
Humanized
Fc modifications
-
Glycoengineering
-
Effector silencing
-
FcγR binding
Retained
C1q binding
Retained
04
Linker & conjugation

Linker chemistry

Linker
-
Class
-
Cleavage
-
Attachment
-
Conjugation
Site-specific
Symmetry
Site-specific (paired)
DAR (mean)
2
DAR homogeneity
Homogeneous
Plasma t½
-
Cleavage trigger
-
Release control
N/A
Hydrophilicity mask
-
Formula
-
Linker MW
-
Linker TPSA
-
Linker xLogP
-
ADCdb linker
-
In-vitro stability
-
05
Payload

Payload & physicochemistry

Payload profile
Payload
MMAE
Class
Auristatin
Mechanism
Tubulin inhibitor
Released catabolite
MMAE (free / unconjugated monomethyl auristatin E)
Mechanistic subtype
Tubulin-auristatin
Stereochem / salt
-
Bystander
Yes
PAMPA rank
-
MW
718 Da
XLogP3
4.1
logD₇.₄
2.7
TPSA
150 Ų
pKa
9.1 pKa
Charge pH 7.4
+1
H-bond donors
4
H-bond acceptors
8
IC50 (HCEC)
-
Formula
C39H67N5O7
PubChem CID
11542188
ADCdb payload
PAY0FSXOW
Hydrophobicity · logD₇.₄
hydrophilic −2+2.7+4 lipophilic
06
Dosing & regimen

Dosing

RP2D dose
4.5 mg/kg
Schedule
Q3W
Route
IV
Fractionated
No
n at RP2D
131
Dose basis
TBW
Trial phase
Phase 1/2
Dose-OAE available
No
Tox summary basis
RP2D
07
Ocular & expression

Ocular profile & eye-tissue target expression

Target profile
OAE any-grade
10 %
OAE grade 3+
2 %
OAE data status
reported
Severity (weighted)
4.4
Keratopathy
-
Conjunctival
-
Dry eye
10 %
Blurred vision
-
Dominant tissue
Cornea
Surface subtype
Corneal (off-target)
Grading scale
CTCAE (unversioned)
Reversibility
Unknown
Target expression in eye tissues (HCA detection · HPA bulk)
Cornea (central)
-
Cornea (limbal)
-
Conjunctiva
-
RPE
-
Retina (HPA)
-
Cross-trial comparability
Ascertainment: Symptom-driven reportingScale: CTCAE (unversioned)Denominator: RP2D⚠ OAE rate not directly comparable across trials
08
Identity & registry

Identifiers, registry & notes

ADC id
jk-06
Approval status
Investigational
Approval year
-
UniProt
Q13641
ADCdb ADC
DRG0CNJHC
ADCdb antibody
-
ADCdb target
TAR0XFYLU
Primary source
ESMO 2025 abstract 961P (Ann Oncol, S0923-7534(25)02450-0); Salubris ASCO 2026 + AACR 2026 press releases (NCT06667960)
Aliases & development codes
JK06; JK 06
Notes
MOLECULE (AACR 2025 abstract 5447): JK-06 is a humanized, quadrivalent/tetravalent biparatopic anti-5T4 (TPBG) ADC built from two mAbs binding distinct 5T4 epitopes — the first clone converted to an scFv and fused to the C-terminal Fc of the second mAb, yielding 4 binding sites across 2 epitopes; DAR2 with stable, site-specific MMAE conjugation; picomolar 5T4 affinity with enhanced internalization. 5T4 = oncofetal Type I transmembrane glycoprotein (limited normal-tissue expression). LINKER UNDISCLOSED: ADCdb (DRG0CNJHC) lists the linker as "Undisclosed" with NO LIN cross-reference id, so all adcdb{} linker physchem fields (SMILES/formula/MW/TPSA/xLogP) and linker_name/class/cleavage/attachment are left blank. MMAE payload implies a cleavable (likely protease/Val-Cit) linker by class analogy, but this is not confirmed in any source, so not asserted. ADCdb also lists antibody name, isotype, and DAR as "Undisclosed"; DAR2, "humanized," and "site-specific" come from the AACR 2025 abstract. THREE DATA CUTS reconciled: (1) ESMO 2025 abstract 961P — dose escalation n=34, 1.5-8.0 mg/kg Q3W IV; only G3+ TRAEs: G3 peripheral neuropathy (1, at 1.5-3.0 mg/kg), G3 keratitis (1, at 4.5 mg/kg), G3 fatigue (1), G3 ALT increase (1), and G5 pneumonitis (1) (last three at 6.0-8.0 mg/kg). (2) AACR 2026 (cutoff 2026-03-29; 153 total / 112 expansion, doses up to 5.2 mg/kg): asthenia 11% was the ONLY AE >10%, all other TRAEs <10%; only 3 G3 events (fatigue, gait disturbance, keratitis); keratitis G3 1/112 (<1%); no G4/5; dose reductions 7/153 (4.6%). (3) ASCO 2026 (cutoff 2026-05-12; 173 total = 42 escalation + 131 expansion at RP2D 4.5 mg/kg) — used for the RP2D ocular/toxicity rows. RP2D = 4.5 mg/kg IV Q3W. RP2D expansion cohort (n=131) TRAEs >=5%: alopecia 15%, asthenia 15%, dry eye 10%, fatigue 10%, nausea 10%. G3 TRAEs: keratitis 2% (n=2), fatigue 1% (n=1), gait disturbance 1% (n=1), neuralgia 1% (n=1); NO G4/G5 TRAEs at RP2D. 3 discontinuations (2%): fatigue, gait disturbance, pneumonitis. PN-driven dose reductions in 2 pts (2%). OCULAR (qualifying signal): dry eye 10% (any grade, most frequent ocular AE, all low-grade) and keratitis G3 2% (n=2). Any-grade keratitis <5% (below the >=5% reporting threshold) yet G3 keratitis = 2% — uncommon but can be severe. dominant_ae_tissue/subtype set to Corneal/Corneal off-target because keratitis is the defining, severe, off-target (MMAE class) corneal event and 5T4 has no notable corneal/conjunctival expression; dry eye (surface) is numerically the most frequent. No ocular AE-related discontinuations; reversibility not explicitly characterized (Unknown). Grading scale = CTCAE, version not stated. dose_oae_available=FALSE (ocular rates essentially reported only at the 4.5 mg/kg RP2D, not across >=2 dose levels). NOT REPORTED (left blank, NOT 0): Hematologic (neutropenia/thrombocytopenia/anemia) and infusion reactions were not among reported TRAEs (i.e., <5%, below threshold) — a notable differentiated, low-myelosuppression MMAE profile, but no documented 0, so cells are blank. Blurred vision and conjunctivitis ocular PTs not reported. Constitutional AEs not mapped to the 7 organ-system buckets (and therefore not made into rows): alopecia 15%, asthenia 11-15%, fatigue 10% (G3 1%), decreased appetite. PCT DERIVATION: dose-escalation single-patient rows (G5 pneumonitis 14.3%, G3 ALT 14.3%, G3 PN 8.3%) report the source's count divided by the source's own dose-binned cohort denominator (1/7, 1/7, 1/12); flagged tier D with raw n in notes. RP2D rows use the percentages stated directly by the source. Annals of Oncology 961P fulltext returned HTTP 403; dose-escalation AE details corroborated via the ADC Review ESMO 2025 coverage and the Salubris ESMO 2025 press release (consistent). Efficacy (context, not required): ESMO NSCLC ORR 38% (5/13); ASCO 2026 squamous NSCLC ORR 50% (5/10) at 4.5 mg/kg, overall squamous NSCLC 35% (6/17)/DCR 94%, EGFRm NSCLC 43%, HR+ breast 30%, TNBC 25%.