Form 8-K

8-K — Lakewood-Amedex Biotherapeutics Inc.

Accession: 0001213900-26-078328

Filed: 2026-07-15

Period: 2026-07-15

CIK: 0002079272

SIC: 2834 (PHARMACEUTICAL PREPARATIONS)

Item: Regulation FD Disclosure

Item: Financial Statements and Exhibits

Documents

8-K — ea0297963-8k_lakewood.htm (Primary)

EX-99.1 — LAKEWOOD-AMEDEX BIOTHERAPEUTICS INC., INVESTOR DECK, DATED JULY 15, 2026 (ea029796301ex99-1.htm)

GRAPHIC (ea029796301_ex99-1img1.jpg)

GRAPHIC (ea029796301_ex99-1img2.jpg)

GRAPHIC (ea029796301_ex99-1img3.jpg)

GRAPHIC (ea029796301_ex99-1img4.jpg)

GRAPHIC (ea029796301_ex99-1img5.jpg)

GRAPHIC (ea029796301_ex99-1img6.jpg)

GRAPHIC (ea029796301_ex99-1img7.jpg)

GRAPHIC (ea029796301_ex99-1img8.jpg)

GRAPHIC (ea029796301_ex99-1img9.jpg)

GRAPHIC (ea029796301_ex99-1img10.jpg)

GRAPHIC (ea029796301_ex99-1img11.jpg)

GRAPHIC (ea029796301_ex99-1img12.jpg)

GRAPHIC (ea029796301_ex99-1img13.jpg)

GRAPHIC (ea029796301_ex99-1img14.jpg)

GRAPHIC (ea029796301_ex99-1img15.jpg)

GRAPHIC (ea029796301_ex99-1img16.jpg)

GRAPHIC (ea029796301_ex99-1img17.jpg)

GRAPHIC (ea029796301_ex99-1img18.jpg)

GRAPHIC (ea029796301_ex99-1img19.jpg)

GRAPHIC (ea029796301_ex99-1img20.jpg)

GRAPHIC (ea029796301_ex99-1img21.jpg)

XML — IDEA: XBRL DOCUMENT (R1.htm)

8-K — CURRENT REPORT

8-K (Primary)

Filename: ea0297963-8k_lakewood.htm · Sequence: 1

false

0002079272

2026-07-15

iso4217:USD

xbrli:shares

iso4217:USD

xbrli:shares

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 OR 15(d) of The Securities

Exchange Act of 1934

Date of Report (Date of earliest event reported):

July 15, 2026

Lakewood-Amedex Biotherapeutics Inc.

(Exact name of registrant as specified in its charter)

Nevada

001-43239

20-5274304

(State or other jurisdiction

of incorporation)

(Commission File Number)

(IRS Employer

Identification No.)

8031 Cooper Creek Blvd., Unit 103

University Park, Florida

34201

(Address of principal executive offices)

(Zip Code)

Registrant’s telephone number, including

area code: (941) 225-2515

N/A

(Former name or former address, if changed since

last report)

Check the appropriate box below if the Form 8-K

filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see

General Instruction A.2. below):

☐

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Rule 12(b) of

the Act:

Title of each class

Trading Symbol(s)

Name of exchange on which registered

Common Stock, par value $0.0001 per share

LABT

The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant

is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the

Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☒

If an emerging growth company, indicate by check

mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting

standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Item

7.01. Regulation FD Disclosure.

On July 15, 2026, Lakewood-Amedex Biotherapeutics

Inc. (the “Company”) made available a corporate investor presentation (the “Investor Deck”) that the Company intends

to use from time to time in meetings and discussions with investors, analysts, and other third parties. The Investor Deck includes, among

other things, the Company's development of Bisphosphocin® compounds, a novel class of fast-acting, broad-spectrum antimicrobials designed

to address drug-resistant infections and the global threat of antimicrobial resistance. It further describes the Company's lead program,

Nu-3, a topically delivered antimicrobial gel selected for clinical development for the treatment of infected diabetic foot ulcers (iDFU),

together with related preclinical and clinical data, regulatory strategy, intellectual property portfolio, competitive landscape, and

management team information.

A copy of the Investor Deck is attached hereto

as Exhibit 99.1 and is incorporated by reference herein.

The information contained in this Current Report

on Form 8-K, including Exhibit 99.1, is being furnished and shall not be deemed to be “filed” for the purposes of Section

18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or incorporated by reference in any filing under

the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

Item 9.01 Financial Statements and Exhibits

(d) Exhibits

Exhibit

Number

Description

99.1

Lakewood-Amedex Biotherapeutics Inc., Investor Deck, dated July 15, 2026

104

Cover Page Interactive Data File (embedded within the Inline XBRL document)

SIGNATURES

Pursuant to the requirements of the Securities

Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

LAKEWOOD-AMEDEX BIOTHERAPEUTICS INC.

Date: July 15, 2026

By:

/s/ Kelvin Cooper

Kelvin Cooper

Chief Executive Officer

EX-99.1 — LAKEWOOD-AMEDEX BIOTHERAPEUTICS INC., INVESTOR DECK, DATED JULY 15, 2026

EX-99.1

Filename: ea029796301ex99-1.htm · Sequence: 2

Exhibit

99.1

Pioneering Bisphosphocin® Compounds Advancing a novel class of fast- acting antimicrobials toaddress the global threat ofresistance 1

Forward-looking Statements This presentation may contain forward-looking statements as defined by the Private Securities Litigation Reform Act of 1995. Generally, the words "believe," "expect," "intends," "estimate," "anticipate," "project," "will" and similar expressions identify forward-looking statements, which generally are not historical in nature. However, the absence of these words or similar expressions does not m e a n that a statement is not forward-looking. All statements that address operating performance, events or developments that we expect or anticipate will occur in the future are forward-looking statements. Management believes that these forward-looking statements are reasonable as and when made. However, caution should be taken not to place undue reliance on any such forward-looking statements because such statements speak only as of the date when made. Our C ompany undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. In addition, forward-looking statements are subject to certain risks and uncertainties that could cause our Company's actual results to differ materially from historical experience and our present expectations or projections. Relying on such statements involves risk, uncertainty and assumptions. These statements are based on the current estimates and assumptions of the ma n a gement of Lakewood‐Amedex Biotherapeutics Inc. as of the date of this press release and are subject to uncertainty and changes. All statements obtained in this press release are ma d e only as of the date of this press release and Lakewood‐Amedex Biotherapeutics Inc. does not undertake any obligation to publicly update any forward‐looking statements. 2

Antimicrobial Resistance (AMR): A Global Public Health Threat Directly causes 1.14 million deaths annually and contributes to nearly 4.7 million deaths worldwide(a) Unaddressed AMR could cost ~$3.8 trillion in lost global G D P by 2050(b) In the U.S., infections from six c o m m o n multidrug-resistant pathogens cost >$4.6B in 2021(c) Core Drivers of AMR 3 • Widespread use of systemic antibiotics • Frequent systemic use of antibiotics for infections suitable for local treatment • Antibiotic use in agriculture Fundamental Barrier • Newly developed systemic antibiotics are vulnerable to resistance • Intended use only as reserve or third-line therapies (a) The Lancet, 2024, 404: 1199-1226, doi.org/10.1016/ S0140-6736(24)01867-1; (b) World Bank Report, 2017; (c) Clinical Infectious Disease, 2021, 72, S17-26.

Value Proposition of Patented Bisphosphocin ® Class First-in-class, antimicrobial compounds with potential to mitigate the impact of the global AMR crisis Broad-spectrum activity against both susceptible and clinically relevant resistant pathogens ( a) Demonstrated cidal activity against biofilm organisms (b) Favorable resistance profile with low risk of resistance development (a) Local delivery achieves high concentration at the site of infection Reduced likelihood of systemic side effects due to targeted delivery 4 (a) –Cooper K, et al, Antimicrobial Agents and Chemotherapy, 2025, https://doi.org/10.1128/aac.00948-25; (b) –Akiyosji D., et al., 53rd ICAAC, 2013, Denver, CO, (abstract F1701a)

Bisphosphocin ® — Proposed Mechanism of Action • Targets bacteria through a pH- and concentration-dependent destabilization of the bacterial cell membrane, typically within one minute of exposure • Broad-spectrum antibacterial activity, including resistant strains (MRSA, VRE), with demonstrated effectiveness against biodefense pathogens Bisphosphocin® compounds are novel, small nucleotide derivatives that are proposed to exert antibacterial activity by targeting bacterial cell membranes, causing rapid bacterial cell death(a) 5 Mechanism of Action – Rapid Destabilization of Bacterial Cell Walls (a)–Cao S.,et al., Ann. Clin. Microbiol. Antimicrob., 2011, 10, 1.

Lead Program: Infected Diabetic Foot Ulcer (iDFU) 6 Global Prevalence • 830M people with diabetes;(a) about one third will develop a DFU ( b ) Infection Rate • ~50% of D FUs become infected; ma ny patients face recurrent events (b) Severe Ou tcomes • Infections are a critical risk factor for amputation, alongside the presence of peripheral arterial disease (b) Resistance Challenge • 15–20% of iDFUs involve resistant pathogens (primarily MRSA) (c) Treatment Shortcomings • Standard-of-care: systemic antibiotics and wound care — yet outcomes remain poor with high recurrence and amputation rates (a) WHO report on diabetes, 2024; (b) Armstrong D., et al., Diabetes Care, 1998, 21 (5), pp 855-859; (c)Zhou S., et al., Metabolic Syndrome and Obesity, 2024, 17, 563-574

Nu-3 Selected for Clinical Development ( a ) Broad spectrum in vitro; Nu-3 shown to be rapidly cidal against a broad spectrum of microbes, including resistant strains, with low potential for resistance development and activity against biofilm Robust efficacy in skin infection models; Nu-3 active as solution or gel formulation in single dose and multiple dose in vivo studies Formulation designed for local administration; Gel formulation developed as most appropriate dosage form for topical application Excellent safety profile toxicology program; minimal effects given at high doses both iv and topical safety studies O pe n IND; Nu-3 IND open and active (a)Cooper K, et al, AntimicrobialAgents and Chemotherapy, 2025, https://doi.org/10.1128/aac.00948-25 7

Nu-3 demonstrates rapid bacterial kill in vitro (a) In the absence of Nu-3 the bacteria are unaffected over the 20-minute time course. 25 m g Vehicle C ontrol At a low concentration (25 mg /ml - 2.5%), all the bacteria are killed within 10 minutes. 50 m g 100 m g At higher concentrations of Nu-3 (50 and 100 mg/ml, 5 and 10%) the bacteria are killed in 5 minutes or less. In time kill experiments, where bacteria are exposed to the Bisphosphocin ® class of compounds, the action is rapid, with total cell death occurring within minutes at higher concentrations a n d lower p H values Time to Kill: Nu-3 vs. E.coli (a)- Cooper K, et al, AntimicrobialAgents and Chemotherapy, 2025, https://doi.org/10.1128/aac.00948-25 8

Nu-3 Gel Formulation Outperforms Solution Formulation(a) 1& 2 Hours At 1 and 2 hours post established infection both 10% gel and 10% solution of Nu-3 show >95% inhibition of MRSA growth 4 Hours At 4 hours post established infection the 10% gel outperforms the 10% solution of Nu-3 in blocking MRSA growth 8 Hours At 8 hours post established infection the 10% gel is far superior to the 10% solution of Nu-3 in blocking MRSA growth (a)- Cooper K, et al, AntimicrobialAgents and Chemotherapy, 2025, https://doi.org/10.1128/aac.00948-25 9 0 10 20 30 40 50 60 70 80 90 100 0 2 4 6 8 Infection as % of Control Hours post Treatment Nu-3 Solution vs Gel in Murine Dermal Infection Model Vehicle 10% Solution 10% Gel

Nu-3 Gel active either once or twice per day in multidose study(a) 5% Gel After 5 days of treatment with 5% Nu-3 gel both once-a-day (QD) and twice-a-day (BID) MRSA growth is >95% inhibited 5% Gel + 5 days recovery After 5 days of treatment plus 5 days recovery with 5% Nu-3 gel the twice-a-day (BID) regimen outperforms the once-a-day regimen in controlling MRSA growth (a)- Cooper K, et al, AntimicrobialAgents and Chemotherapy, 2025, https://doi.org/10.1128/aac.00948-25 10 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100% Infection as % of Conrtol 5-Day Multiple Dose Mouse Infection Model BID QD Control 5-Days Treatment 5-Days Treatment + 5-Days Recovery

Advantages of Bisphosphocin ® Class in Com bat ing AMR: based on available non-clinical evidence 11 Right Drug Right Application Right MOA

Clinical Evidence Supporting Development of Nu-3 • A 21‐Day Repeat Patch Test to Evaluate the Irritation Potential of Test Product (2% Nu‐3 in 0.85% Saline, W/V) on Abraded and Intact Skin Sites with Controls • 35 healthy subjects exposed • Abraded skin: Positive control > 2% Nu‐3 > Negative saline solution control • Intact skin: Positive control > 2% Nu‐3 = Negative saline solution control • Double blinded, randomized, dose‐escalating • Doses of Nu‐3 solution: 0.1%, 1% and 2 % or placebo (8:8:8:6 randomization) • 30 patients analyzed • Safety as primary endpoint • Efficacy secondary: pathogen reduction and ulcer surface area measurements 12 Phase 1 Patch Study Exploratory Phase 2a Study in Patients with iDFU

Step One: Phase 2a Study SINGLE Blinded, R an d om ized Nu-3 gel 2% Nu-3 gel 5% Nu-3 gel 10% Active Treatment D ay 1 Day 14 Day 28 Follow u p N o treatment N o treatment N o treatment Step Two: Phase 2b Study 13 U p c o m i n g Phase 2a/2b Study Design with N e w Gel Formulation Indication • Infected diabetic foot ulcers Safety Measures • Number of related AEs and SAEs Efficacy Measures • Reduction in C F U at days 7 and 14 compared to baseline • Clinical infection scores and wound size changes Protocol • Phase 2a: Aligned with F D A comments • Phase 2b: F D A reviewed and in alignment – NCT0602035 (ClinicalTrials.gov) Target Outcome • Achieve clinical proof-of-concept of safety and antimicrobial efficacy in Phase 2 *Treatment groups in Phase 2b will be confirmed after Phase 2a readout D O U B L E Blinded, R an d om ized Nu-3 gel 5% Nu-3 gel 10% Placebo Active Treatment D ay 1 Day 14 Day 28 Follow u p N o treatment N o treatment N o treatment

iDFU Development and Regulatory Strategy 14 Geographic Scope • Phase 2 U.S.development • Phase 3 International development Clinical Development • 2 small accessory studies full pharmacokinetic and skin sensitization • E n d of Phase 2 Meeting • Phase 3: In partnership to attain global reach and capabilities o Active comparator trial(s) o Longer follow-up in Phase 3 to establish clinical utility on wound healing (Performance + Utility) Manufacturing Final Formulation at end of Phase 2 • Defining the commercial application for Phase 3 • Application system will determine drug or combination drug-device development path

N u -3 N u -8 N u -11 N u -10 Indication P rogram : Discovery Pre-clinical Phase 1 Phase 2 Phase 3 Status Targe ts: • Pulmonary Infections • Urinary Tract Infections • Oral Mucositis • Otitis Externa Skin and Soft tissue Infections (SSTI), e.g., Infected Diabetic Foot Ulcers (iDFU) Phase 2initiation Profiling for potential indication development Development Pipeline 15

Upcoming Milestones 2Q26 • Drug product manufacturing initiated • Site enrollment initiated 16 3Q26 • Drug product manufacturing completed • Site enrollment completed • Clinical Trial Commences • First Patient First Visit 4Q26 • Clinical Trial Complete • Last Patient Last Visit 4Q26/1Q27 • Top Line Results

Robust Intellectual Property Portfolio 71 Issu ed 30 P e ndin g 101 Patents 17 Patent Exclusivity • Key filings provide protection through 2038 • Recent applications extend through 2044 Patent Coverage • Patents cover composition-of-matter of the Bisphosphocin ® class and other related classes of compounds; formulations of Nu-3; use patents for the Bisphosphocin ® class; and process patents for the class

Nu-3 Well Positioned in Competitive Landscape 18 Only One Direct and Comparable Competitor – Recce's R327 • Topical agent for Skin & Soft Tissue Infections – focus on iDFU • Late-stage development in Australia & Indonesia • No approved topical for treatment of iDFU • No efficacy against resistant pathogens Proprietary Topical Standard of Care OTC • Effect of oral antibiotics in mild iDFU not demonstrated • Guidelines based on general infection stewardship

Experienced Management with Industry Depth Kelvin Cooper, Ph.D. Chief Executive Officer • 45 Years in the Pharmaceutical Industry • 30 years at Pfizer • Executive Leadership roles in D r u g Discovery, D r u g Development, Manufacturing, and Commercial Peter C e c ca c c i Chief Financial Officer • More than 25 years of experience as a Senior Executive with comprehensive experience in accounting, finance, strategy, compliance, and m a n a g e m e n t T h o m a s Balzer, M.D., Ph.D. Chief Medical Officer • 30 Years in the Pharmaceutical Industry at Schering AG, Bayer US, Exact Sciences • Executive Leadership roles in Global Clinical Development and Global Medical Affairs at Bayer U S L eadership B o ard Kelvin Cooper, Ph.D. Chief Executive Officer L eonard J. D e R o m a Director D o u g Manion, M.D., F RC P ( C ) Chairman J o s e p h Tucker, Ph.D. Director 19

Pioneering Innovations to Com bat Drug-Resistant Infections Clinical-stage biotechnology co m p a ny developing a novel class of fast-acting, broad-spectrum antimicrobials — Bisphosphocin ® comp ou n d s — to treat infectious diseases a n d reduce the threat posed by antibiotic-resistant microbes Phase 2-ready lead product, Nu-3, is a topically delivered antimicrobial gel for the treatment of infected diabetic foot ulcers (iDFU) Pre-clinical or early clinical data demonstrate broad, fast-acting activity (incl. resistant strains) with low resistance risk, a favorable safety profile, and effective local action Potential first-in-class infection therapy for the treatment of iDFU Near-term milestones include the initiation of a planned Phase 2a clinical trial evaluating the safety and efficacy of Nu-3 in iDFU Robust intellectual property estate with key filings providing protection through 2038 and recent applications extending through 2044 20

GRAPHIC

Filename: ea029796301_ex99-1img1.jpg · Sequence: 3

Binary file (446889 bytes)

Download ea029796301_ex99-1img1.jpg

GRAPHIC

Filename: ea029796301_ex99-1img2.jpg · Sequence: 4

Binary file (626627 bytes)

Download ea029796301_ex99-1img2.jpg

GRAPHIC

Filename: ea029796301_ex99-1img3.jpg · Sequence: 5

Binary file (395379 bytes)

Download ea029796301_ex99-1img3.jpg

GRAPHIC

Filename: ea029796301_ex99-1img4.jpg · Sequence: 6

Binary file (340820 bytes)

Download ea029796301_ex99-1img4.jpg

GRAPHIC

Filename: ea029796301_ex99-1img5.jpg · Sequence: 7

Binary file (417946 bytes)

Download ea029796301_ex99-1img5.jpg

GRAPHIC

Filename: ea029796301_ex99-1img6.jpg · Sequence: 8

Binary file (351042 bytes)

Download ea029796301_ex99-1img6.jpg

GRAPHIC

Filename: ea029796301_ex99-1img7.jpg · Sequence: 9

Binary file (309726 bytes)

Download ea029796301_ex99-1img7.jpg

GRAPHIC

Filename: ea029796301_ex99-1img8.jpg · Sequence: 10

Binary file (304161 bytes)

Download ea029796301_ex99-1img8.jpg

GRAPHIC

Filename: ea029796301_ex99-1img9.jpg · Sequence: 11

Binary file (322712 bytes)

Download ea029796301_ex99-1img9.jpg

GRAPHIC

Filename: ea029796301_ex99-1img10.jpg · Sequence: 12

Binary file (306780 bytes)

Download ea029796301_ex99-1img10.jpg

GRAPHIC

Filename: ea029796301_ex99-1img11.jpg · Sequence: 13

Binary file (183295 bytes)

Download ea029796301_ex99-1img11.jpg

GRAPHIC

Filename: ea029796301_ex99-1img12.jpg · Sequence: 14

Binary file (302010 bytes)

Download ea029796301_ex99-1img12.jpg

GRAPHIC

Filename: ea029796301_ex99-1img13.jpg · Sequence: 15

Binary file (397346 bytes)

Download ea029796301_ex99-1img13.jpg

GRAPHIC

Filename: ea029796301_ex99-1img14.jpg · Sequence: 16

Binary file (276960 bytes)

Download ea029796301_ex99-1img14.jpg

GRAPHIC

Filename: ea029796301_ex99-1img15.jpg · Sequence: 17

Binary file (174717 bytes)

Download ea029796301_ex99-1img15.jpg

GRAPHIC

Filename: ea029796301_ex99-1img16.jpg · Sequence: 18

Binary file (197715 bytes)

Download ea029796301_ex99-1img16.jpg

GRAPHIC

Filename: ea029796301_ex99-1img17.jpg · Sequence: 19

Binary file (232006 bytes)

Download ea029796301_ex99-1img17.jpg

GRAPHIC

Filename: ea029796301_ex99-1img18.jpg · Sequence: 20

Binary file (285359 bytes)

Download ea029796301_ex99-1img18.jpg

GRAPHIC

Filename: ea029796301_ex99-1img19.jpg · Sequence: 21

Binary file (303006 bytes)

Download ea029796301_ex99-1img19.jpg

GRAPHIC

Filename: ea029796301_ex99-1img20.jpg · Sequence: 22

Binary file (337618 bytes)

Download ea029796301_ex99-1img20.jpg

GRAPHIC

Filename: ea029796301_ex99-1img21.jpg · Sequence: 23

Binary file (379576 bytes)

Download ea029796301_ex99-1img21.jpg

XML — IDEA: XBRL DOCUMENT

XML

Filename: R1.htm · Sequence: 28

v3.26.1

Cover

Jul. 15, 2026

Cover [Abstract]

Document Type

8-K

Amendment Flag

false

Document Period End Date

Jul. 15, 2026

Entity File Number

001-43239

Entity Registrant Name

Lakewood-Amedex Biotherapeutics Inc.

Entity Central Index Key

0002079272

Entity Tax Identification Number

20-5274304

Entity Incorporation, State or Country Code

Entity Address, Address Line One

8031 Cooper Creek Blvd.

Entity Address, Address Line Two

Unit 103

Entity Address, City or Town

University Park

Entity Address, State or Province

Entity Address, Postal Zip Code

34201

City Area Code

941

Local Phone Number

225-2515

Written Communications

false

Soliciting Material

false

Pre-commencement Tender Offer

false

Pre-commencement Issuer Tender Offer

false

Title of 12(b) Security

Common Stock, par value $0.0001 per share

Trading Symbol

LABT

Security Exchange Name

NASDAQ

Entity Emerging Growth Company

true

Elected Not To Use the Extended Transition Period

false

- Definition

Boolean flag that is true when the XBRL content amends previously-filed or accepted submission.

+ References

No definition available.

+ Details

Name:

dei_AmendmentFlag

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Area code of city

+ References

No definition available.

+ Details

Name:

dei_CityAreaCode

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Cover page.

+ References

No definition available.

+ Details

Name:

dei_CoverAbstract

Namespace Prefix:

dei_

Data Type:

xbrli:stringItemType

Balance Type:

Period Type:

duration

- Definition

For the EDGAR submission types of Form 8-K: the date of the report, the date of the earliest event reported; for the EDGAR submission types of Form N-1A: the filing date; for all other submission types: the end of the reporting or transition period. The format of the date is YYYY-MM-DD.

+ References

No definition available.

+ Details

Name:

dei_DocumentPeriodEndDate

Namespace Prefix:

dei_

Data Type:

xbrli:dateItemType

Balance Type:

Period Type:

duration

- Definition

The type of document being provided (such as 10-K, 10-Q, 485BPOS, etc). The document type is limited to the same value as the supporting SEC submission type, or the word 'Other'.

+ References

No definition available.

+ Details

Name:

dei_DocumentType

Namespace Prefix:

dei_

Data Type:

dei:submissionTypeItemType

Balance Type:

Period Type:

duration

- Definition

Address Line 1 such as Attn, Building Name, Street Name

+ References

No definition available.

+ Details

Name:

dei_EntityAddressAddressLine1

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Address Line 2 such as Street or Suite number

+ References

No definition available.

+ Details

Name:

dei_EntityAddressAddressLine2

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Name of the City or Town

+ References

No definition available.

+ Details

Name:

dei_EntityAddressCityOrTown

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Code for the postal or zip code

+ References

No definition available.

+ Details

Name:

dei_EntityAddressPostalZipCode

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Name of the state or province.

+ References

No definition available.

+ Details

Name:

dei_EntityAddressStateOrProvince

Namespace Prefix:

dei_

Data Type:

dei:stateOrProvinceItemType

Balance Type:

Period Type:

duration

- Definition

A unique 10-digit SEC-issued value to identify entities that have filed disclosures with the SEC. It is commonly abbreviated as CIK.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection b-2

+ Details

Name:

dei_EntityCentralIndexKey

Namespace Prefix:

dei_

Data Type:

dei:centralIndexKeyItemType

Balance Type:

Period Type:

duration

- Definition

Indicate if registrant meets the emerging growth company criteria.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection b-2

+ Details

Name:

dei_EntityEmergingGrowthCompany

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Indicate if an emerging growth company has elected not to use the extended transition period for complying with any new or revised financial accounting standards.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Securities Act

-Number 7A

-Section B

-Subsection 2

+ Details

Name:

dei_EntityExTransitionPeriod

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Commission file number. The field allows up to 17 characters. The prefix may contain 1-3 digits, the sequence number may contain 1-8 digits, the optional suffix may contain 1-4 characters, and the fields are separated with a hyphen.

+ References

No definition available.

+ Details

Name:

dei_EntityFileNumber

Namespace Prefix:

dei_

Data Type:

dei:fileNumberItemType

Balance Type:

Period Type:

duration

- Definition

Two-character EDGAR code representing the state or country of incorporation.

+ References

No definition available.

+ Details

Name:

dei_EntityIncorporationStateCountryCode

Namespace Prefix:

dei_

Data Type:

dei:edgarStateCountryItemType

Balance Type:

Period Type:

duration

- Definition

The exact name of the entity filing the report as specified in its charter, which is required by forms filed with the SEC.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection b-2

+ Details

Name:

dei_EntityRegistrantName

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

The Tax Identification Number (TIN), also known as an Employer Identification Number (EIN), is a unique 9-digit value assigned by the IRS.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection b-2

+ Details

Name:

dei_EntityTaxIdentificationNumber

Namespace Prefix:

dei_

Data Type:

dei:employerIdItemType

Balance Type:

Period Type:

duration

- Definition

Local phone number for entity.

+ References

No definition available.

+ Details

Name:

dei_LocalPhoneNumber

Namespace Prefix:

dei_

Data Type:

xbrli:normalizedStringItemType

Balance Type:

Period Type:

duration

- Definition

Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 13e

-Subsection 4c

+ Details

Name:

dei_PreCommencementIssuerTenderOffer

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 14d

-Subsection 2b

+ Details

Name:

dei_PreCommencementTenderOffer

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Title of a 12(b) registered security.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection b

+ Details

Name:

dei_Security12bTitle

Namespace Prefix:

dei_

Data Type:

dei:securityTitleItemType

Balance Type:

Period Type:

duration

- Definition

Name of the Exchange on which a security is registered.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection d1-1

+ Details

Name:

dei_SecurityExchangeName

Namespace Prefix:

dei_

Data Type:

dei:edgarExchangeCodeItemType

Balance Type:

Period Type:

duration

- Definition

Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as soliciting material pursuant to Rule 14a-12 under the Exchange Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 14a

-Subsection 12

+ Details

Name:

dei_SolicitingMaterial

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration

- Definition

Trading symbol of an instrument as listed on an exchange.

+ References

No definition available.

+ Details

Name:

dei_TradingSymbol

Namespace Prefix:

dei_

Data Type:

dei:tradingSymbolItemType

Balance Type:

Period Type:

duration

- Definition

Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as written communications pursuant to Rule 425 under the Securities Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Securities Act

-Number 230

-Section 425

+ Details

Name:

dei_WrittenCommunications

Namespace Prefix:

dei_

Data Type:

xbrli:booleanItemType

Balance Type:

Period Type:

duration