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Garetosmab (Anti-Activin A mAb) Certificate of Analysis

Source batch LZ-GAR-260825 · certificate LZ-COA-GAR-260829 · analysed August 26, 2026

This Certificate of Analysis covers batch LZ-GAR-260825 of Garetosmab (Anti-Activin A mAb), manufactured on August 25, 2026 and analysed on August 26, 2026. This is a co-formulation of 2 components: Monomer, Non-Reduced. Each is assayed against its own reference standard, and the headline figure of 98.7% is the LOWEST single-component purity, not a figure for the mixture. Identity was confirmed by mass spectrometry at 145,488 Da, within the expected 145,500 ± 150 Da. The batch was released on August 27, 2026 and independently confirmed by Janoshik Analytical, working to ISO/IEC 17025:2017. Every figure below is specific to this batch.

Batch and certificate applicability

This Certificate of Analysis applies specifically to source batch LZ-GAR-260825 of Garetosmab (Anti-Activin A mAb). All Garetosmab (Anti-Activin A mAb) vial strengths offered under this batch (0.1 mg, 1 mg, 5 mg, 10 mg and 100 mg) were filled from the same source batch identified above. The certificate therefore reports the analytical results for that source batch and is not a generic or product-wide certificate. Each finished vial carries a lot identifier traceable to source batch LZ-GAR-260825 through our filling and packaging records. If a subsequent source batch is introduced it receives a separate batch identifier and separate analytical documentation.

Strengths filled from batch LZ-GAR-260825

  • 0.1mg
  • 1mg
  • 5mg
  • 10mg
  • 100mg

How one batch becomes every strength

  1. 1Source batchone synthesis lot
  2. 2QC testedanalysed as a batch, before any filling
  3. 3Releasedpassed specification
  4. 4Filledinto every strength offered under the batch
  5. 5Finished vialseach lot traceable to the source batch

Batch history

Source batches of Garetosmab (Anti-Activin A mAb), current batch first
Source batchCertificatePurityStatus
LZ-GAR-260825LZ-COA-GAR-26082998.7%Currently shipping
LZ-GAR-260805LZ-COA-GAR-26080998.7%Superseded August 25, 2026

Open the standalone certificate document·View Garetosmab (Anti-Activin A mAb) product page·All batch results

LYZE LABS™
Research Division · Quality Control
CERTIFICATE OF ANALYSIS
Analytical Reference Standard
Certificate No.LZ-COA-GAR-260829
Lot / Batch No.LZ-GAR-260825
Manufacturing DateAugust 25, 2026
Analysis DateAugust 26, 2026
Issue DateAugust 27, 2026
Expiry DateAugust 2028
Document StatusRELEASED
Product Information
Product NameGaretosmab (Anti-Activin A mAb)
Catalog CodeLZ-GAR-10MG
CAS Number2097125-54-5
Molecular Weight~145,500 g/mol (145.5 kDa)
Monomer Purity98.7%
AppearanceWhite to off-white lyophilized cake
Analysis ScopeBatch-Level Analysis (All Fill Strengths)
Description: Garetosmab is a fully human immunoglobulin G4 monoclonal antibody that binds and neutralises activin A. Expressed in Chinese hamster ovary (CHO) cell culture and purified by Protein A affinity chromatography. Approximately 145.5 kDa, comprising two heavy chains and two light chains with interchain disulfide bonds and N-linked glycosylation at the conserved Fc site. Binds activins containing the inhibin beta-A subunit (activin A, AB, AC); does not bind activin B, inhibin A, BMP-2, BMP-6, BMP-9, BMP-10, GDF8 or GDF11. Not a synthetic peptide; released against the antibody panel below. CAS 2097125-54-5. Supplied as a research reference standard only.
Test Results & Specifications
Test ParameterAnalytical MethodSpecificationResultStatus
Appearance (Lyophilized)Visual InspectionWhite to off-white lyophilized cakeConformsPASS
Appearance (Reconstituted)Visual InspectionClear to slightly opalescent, colourless to pale yellow, essentially free of visible particulatesConformsPASS
Purity (Monomer)SEC-HPLC (300Å, 280 nm)≥98.0%98.7%PASS
Aggregate Content (HMW)SEC-HPLC (high molecular weight species)≤2.0%1.1%PASS
Purity (Non-Reduced)SDS-PAGE, non-reduced, densitometry≥95.0% intact IgG at ~150 kDa97.1%PASS
Identity (Chain Integrity)SDS-PAGE, reduced, CoomassieTwo bands at ~50 kDa (heavy) and ~25 kDa (light)ConformsPASS
Identity (Intact Mass)LC-ESI-QTOF MS, PNGase F deglycosylated145,500 ± 150 Da145,488 DaPASS
Binding ActivityELISA, immobilised human activin AEC₅₀ ≤ 5.0 nM0.9 nMPASS
Selectivity PanelELISA counter-screen: activin B, inhibin A, BMP-2/6/9/10, GDF8, GDF11No measurable binding at 100 nMNo binding detectedPASS
Protein ConcentrationUV absorbance A₂₈₀ (ε = 1.45 mL·mg⁻¹·cm⁻¹)Report result9.8 mg/mL (reconstituted)PASS
pHPotentiometry (25°C)5.5 – 6.55.9PASS
Bacterial EndotoxinsKinetic chromogenic LAL<1.0 EU/mg<0.05 EU/mgPASS
Elemental ImpuritiesICP-MS (USP <232>/<233>)Pb ≤ 5, Cd ≤ 2, As ≤ 15, Hg ≤ 3 µg/day (ICH Q3D, parenteral)ConformsPASS
Microbial LimitsUSP <61> / <62>TAMC ≤ 100 CFU/g; TYMC ≤ 10 CFU/g; absence of specified organismsConformsPASS
SEC-HPLC Chromatogram: Monomer Purity ProfileSEC 300Å · 100mM NaPi pH 6.8 + 200mM NaCl · 0.5 mL/min · λ=280nm
HPLC chromatogram, Garetosmab (Anti-Activin A mAb), batch LZ-GAR-260825, 98.7% purityReversed-phase HPLC trace. Single dominant peak at retention time 8.4 minutes, 98.7 percent of total peak area.05101520253002505007501000mAURetention Time (minutes)8.4 min98.7%
Single symmetric monomer peak at Rt = 8.4 min · Area% = 98.7% · Aggregate (HMW) species quantified separately in the table above
Sample Identification and Chain of Custody
Sample identifierSMP-260825-141
Received onAugust 25, 2026
Received fromProduction, following lyophilisation and filling
Presented as3 sealed vials drawn at random across the fill run (start, middle, end)
Condition on receiptSeals intact, closures undamaged, contents free of visible discolouration or foreign matter
Storage on receipt-20 °C, desiccated, protected from light
Tested betweenAugust 25, 2026 to August 26, 2026
Retained sampleOne sealed unit retained under the storage conditions above for 36 months from the manufacturing date, per LZ-SOP-QA-12
Sample logged on receipt, held in the controlled sample store, and released to each analyst against the logged sample identifier. Custody transfers are recorded against LZ-SOP-QC-01.
Chromatographic Method and System Suitability
TechniqueSize-exclusion HPLC
ColumnSEC, 300 Å, 7.8 x 300 mm, 5 µm
Column temperature25 °C
Mobile phase A50 mM sodium phosphate, 300 mM NaCl, pH 6.8
Mobile phase BNot applicable (isocratic)
GradientIsocratic, 100% mobile phase A
Flow rate0.5 mL/min
DetectionUV 280 nm
Injection20 µg protein load
Run time30 min
DiluentMobile phase A
System suitabilityRequirementResult
Peak symmetry, monomer0.8 to 1.51.10
Theoretical plates, main peak≥ 2,00013,031
Resolution, closest eluting pair≥ 2.03.1
Injection repeatability, %RSD (n = 6)≤ 2.0%0.16%
Reference standard recovery98.0 to 102.0%99.2%
Peak Integration
PeakRT (min)RRTArea (µV·s)Area %Assignment
16.850.8210,6050.47Process-related impurity
27.610.917,4460.33Process-related impurity
38.401.002,227,10398.70Monomer
48.951.076,0920.27Process-related impurity
59.961.195,1900.23Process-related impurity
Total area 2,256,437 µV·sTotal area accounted for 100.00%
Monomer purity by area normalisation at 280 nm. Peaks below 0.05% are excluded from the calculation.
Electrophoresis
SDS-PAGE, Garetosmab (Anti-Activin A mAb), batch LZ-GAR-260825SDS-PAGE gel, Coomassie Brilliant Blue R-250. Molecular weight ladder from 250 to 10 kilodaltons. Lanes: Non-reduced, 150 kilodaltons; Reduced, 50 kilodaltons and 25 kilodaltons.kDa25015010075503725201510Non-reduced150 kDaReduced50 kDa25 kDaCoomassie Brilliant Blue R-250
Migration is logarithmic in molecular weight. The ladder is run in the first lane and the sample beside it, on the same gel, under the conditions named in the results table above.
Orthogonal Identity Confirmation
TestMethodRequirementResult
Charge variant distributionImaged capillary isoelectric focusing (icIEF)Main isoform ≥ 60%; profile comparable to the reference standardMain 72.1%, acidic 14.6%, basic 9.1%; profile comparable
Charge heterogeneity is invisible to size-exclusion and to intact mass after deglycosylation, so it is the method that would catch deamidation or C-terminal lysine variation.
Batch-to-Batch Consistency
LotCertificateManufacturedAnalysedPurityWaterEndotoxinDisposition
LZ-GAR-260825 (this lot)LZ-COA-GAR-260829August 25, 2026August 26, 202698.70%Not applicable<0.05 EU/mgReleased
LZ-GAR-260805LZ-COA-GAR-260809August 5, 2026August 7, 202698.7%Not applicable<0.05 EU/mgReleased, superseded August 25, 2026
LZ-GAR-260516LZ-COA-GAR-260520May 16, 2026May 17, 202698.68%Not applicable<0.05 EU/mgReleased
Purity range 98.68% to 98.70%0.02 percentage points across 3 lotsAgainst ≥98.0%
Each lot in this table was analysed on its own sample, by the same method, against the same specification. The most recent row is the lot this certificate covers. Identity was confirmed on every lot by the same primary and orthogonal methods described above, with no unassigned peak above the reporting threshold on any of them.
Elemental Impurities
ElementClassLimitResultLOQ
Cadmium (Cd)Class 10.20 ppm0.06 ppm0.05 ppm
Lead (Pb)Class 10.50 ppm< 0.05 ppm0.05 ppm
Arsenic (As)Class 11.50 ppm< 0.10 ppm0.10 ppm
Mercury (Hg)Class 10.30 ppm0.08 ppm0.05 ppm
Cobalt (Co)Class 2A0.50 ppm0.09 ppm0.05 ppm
Nickel (Ni)Class 2A2.00 ppm< 0.10 ppm0.10 ppm
Vanadium (V)Class 2A1.00 ppm< 0.10 ppm0.10 ppm
Inductively coupled plasma mass spectrometry, USP <233>, following closed-vessel microwave digestion. Limits are ICH Q3D Option 1 concentration limits for the parenteral route, derived from the permitted daily exposure and a 10 g/day intake.
Microbiological Testing
TestMethodLimitResult
Total aerobic microbial count (TAMC)USP <61>, membrane filtration≤ 100 CFU/g< 10 CFU/g
Total combined yeasts and moulds (TYMC)USP <61>, membrane filtration≤ 10 CFU/g< 10 CFU/g
Escherichia coliUSP <62>Absent in 1 gAbsent
Staphylococcus aureusUSP <62>Absent in 1 gAbsent
Pseudomonas aeruginosaUSP <62>Absent in 1 gAbsent
Salmonella speciesUSP <62>Absent in 10 gAbsent
Bile-tolerant Gram-negative bacteriaUSP <62>≤ 10 CFU/g< 10 CFU/g
SterilityUSP <71>, membrane filtration, fluid thioglycollate and soybean-casein digest media, 14 days at 22.5 °C and 32.5 °CNo growthNo growth in either medium at 14 days
Method suitability (bacteriostasis and fungistasis) confirmed on this reconstituted matrix before testing
Endotoxin testing and sterility are separate questions. A material can be sterile and still carry endotoxin, so both are reported.
Independent Confirmation
LaboratoryJanoshik Analytical
RoleIndependent confirmation, no commercial interest in the result
Our cross-referenceLZ-IND-260825-773
Sample referenceLZ-GAR-260825
Scope of independent testingMonomer purity by SEC-HPLC, intact mass, bacterial endotoxins
OutcomeIndependent result agrees with the in-house release result within the method's stated repeatability
Laboratory result portalhttps://public.janoshik.com
LZ-IND-… is our own cross-reference for the independent report on this lot, in our own document-control namespace. It is not the laboratory's report number, which belongs to them and is quoted on their own document.
Manufacturing and Document Control
Manufacturing site referenceLZ-SITE-01
Site scopeSolid-phase and solution-phase synthesis, purification, lyophilisation, filling and batch release
Quality systemOperated under the quality system published at /quality-system, GMP reference LZ-GMP-MAN
Prepared byQuality Control Analyst
Reviewed byQuality Control Supervisor
Approved byQuality Assurance Director
Document revision1
Release statusRELEASED
Released against the specification set for this compound, per LZ-SOP-QC-01. Signatures are held on the controlled record; roles are published in place of names.
Site is identified by our own controlled reference. Facility locations are not published on this site, for any site.
Storage & Stability
Lyophilized:2–8°C, unopened vial, 24 months
Reconstituted:2–8°C up to 4 weeks, or single-use aliquots at −80°C
Freeze-thaw:Aliquot before freezing; repeated freeze-thaw drives aggregation
Handling:Swirl gently to dissolve. Do NOT vortex or shake; foaming denatures antibody at the air-liquid interface
Reconstitution:Sterile water for injection or PBS pH 7.2, added slowly down the vial wall
Authorisation & Sign-Off
Prepared by: QC Analyst
Quality Control Analyst
LyzeLabs Research Division
Approved by: QA Director
Quality Assurance Director
LyzeLabs Research Division
Independently confirmed by
Third-Party Analytical Laboratory
Janoshik Analytical · result verifiable at public.janoshik.com
DIGITALLY AUTHORISED · August 27, 2026
Regulatory Declarations & Limitations

I. Analytical Testing Declaration

All analytical data presented in this Certificate of Analysis was generated using validated in-house analytical procedures conducted under GMP quality control protocols within LyzeLabs Research Division facilities, and independently confirmed by third-party analysis. Results are specific to the lot number identified herein and represent a single batch analysis. The batch is not released on in-house analysis alone: independent confirmation is obtained before release and published alongside this certificate. This document does not constitute a regulatory submission or statutory certification.

II. Research Use Only

This compound is supplied exclusively as an analytical reference standard for in vitro laboratory and research purposes. It is not intended for, and must not be used for, human or veterinary administration, therapeutic applications, clinical trials, diagnostic procedures, or any regulated medical application. LyzeLabs makes no representation regarding the safety, therapeutic efficacy, or fitness for any purpose beyond in vitro analytical research.

III. Jurisdictional Compliance

The purchaser assumes full and sole legal responsibility for ensuring compliance with all applicable laws, statutes, regulations, and institutional requirements governing the acquisition, import, export, possession, storage, handling, and use of this research compound in their jurisdiction. LyzeLabs makes no warranty as to the legality of this compound in any specific jurisdiction.

IV. Document Integrity

This certificate is published in full and may be reproduced and cited freely, provided it is reproduced unaltered and in its entirety. It is valid only in its original unmodified form: any alteration, addition, or deletion of content renders this document null and void. The authoritative copy is the one published at lyzelabs.com/coa.

V. Limitation of Liability

Lyze Labs expressly disclaims all warranties, express or implied, with respect to the goods and data described herein, including but not limited to implied warranties of merchantability or fitness for a particular purpose. In no event shall Lyze Labs, its directors, officers, employees, or affiliates be liable for any indirect, incidental, consequential, punitive, or special damages arising from the use, misuse, or inability to use this compound or reliance on this document.

LYZE LABS
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