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Marshall Edwards, Inc.

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uuid002o98t

Namestring
Marshall Edwards, Inc.
Legal namestring
Marshall Edwards, Inc.
Company typeenum
Public
Founded yearint
2000
Descriptiontext

Marshall Edwards, Inc. is a clinical-stage oncology company headquartered in San Diego, California, that develops novel anti-cancer therapeutics derived from an isoflavone-based chemistry platform originally licensed from its majority shareholder and Australian parent, Novogen Limited (ASX:NRT). The company was incorporated in Delaware in December 2000, began trading on Nasdaq (ticker: MSHL) in December 2003, and relocated its headquarters from Sydney to San Diego in April 2010 following the appointment of Dr. Daniel Gold as CEO. The lead pipeline is organized around two complementary mechanisms targeting tumor cell metabolism: the NADH oxidase inhibitor program (lead candidate ME-143, with first-generation Phenoxodiol and Triphendiol precursors) and the mitochondrial inhibitor program (lead candidate ME-344, with first-generation NV-128 precursor). The platform has generated more than 400 synthetic chemical structures based on naturally-occurring plant isoflavones, and the company holds exclusive worldwide rights through an IP portfolio of 11 issued U.S. patents, 40+ foreign patents, and 80+ foreign applications acquired from Novogen in May 2011.

The core technology targets cancer cell metabolism through two distinct pathways — ME-143 inhibits the sphingosine kinase-Akt signaling pathway to induce caspase-mediated apoptosis, while ME-344 induces caspase-independent cell death via DNA fragmentation and destructive autophagy by targeting the terminal respiratory chain complex. ME-143 entered a Phase I clinical trial in September 2011 for patients with refractory solid tumors, and ME-344 demonstrated tenfold greater anti-tumor activity than NV-128 in preclinical studies, with an IND application filed in Q1 2012. Marshall Edwards is a pre-revenue, publicly traded development-stage company with 11–50 employees, no commercial products, and no product pricing. Its stated go-to-market is the completion of early-stage clinical trials followed by out-licensing or partnering with pharmaceutical companies for late-stage development and commercialization; its primary customers, when commercial, will be oncology healthcare institutions and patients with chemotherapy-resistant cancers including platinum/taxane-refractory ovarian cancer, KRAS-mutant NSCLC, and prostate cancer. Capital to date has been sourced primarily through a December 2011 $2 million private placement from Novogen Limited, supplemented by periodic equity offerings to fund ongoing R&D and clinical operations.

Short descriptiontext

Marshall Edwards, Inc. is a San Diego-based clinical-stage oncology company developing isoflavone-based anti-cancer therapeutics, with lead candidates ME-143 (NADH oxidase inhibitor in Phase I) and ME-344 (mitochondrial inhibitor) targeting chemotherapy-resistant solid tumors for eventual out-licensing to pharmaceutical partners.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage oncology, anti-cancer therapeutics, isoflavone drug platform, NADH oxidase inhibitors, mitochondrial inhibitors
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Oncology Therapeutics
No data
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Private Placement Financing
TypeOne Time License
Description

The company raises capital through private placement offerings. In December 2011, the company sold approximately 1.94 million shares of common stock to its majority shareholder Novogen Limited for gross proceeds of $2 million.

marshalledwardsinc.com
2Future Product Revenue
TypeLicensing Royalties
Description

Pre-revenue clinical stage company planning to commercialize drug candidates through partnering agreements with pharmaceutical companies upon successful clinical development and regulatory approval.

marshalledwardsinc.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Marshall Edwards, Inc. is a clinical-stage oncology company developing novel anti-cancer therapeutics based on an isoflavone technology platform derived from naturally occurring plant compounds. The company's lead programs focus on two families of small molecules that target tumor cell metabolism: the NADH oxidase inhibitor program led by ME-143, and the mitochondrial inhibitor program led by ME-344, supported by first-generation compounds Phenoxodiol, NV-128, and Triphendiol.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • ME-143 demonstrated superior anti-tumor activity against a broad range of tumor cell lines compared to Phenoxodiol and Triphendiol in pre-clinical studies
+2 more records
Product overview1 text field

Marshall Edwards is a San Diego-based oncology company developing a pipeline of novel anti-cancer therapeutics derived from an isoflavone technology platform. The company's lead programs focus on two families of small molecules targeting tumor cell metabolism: the NADH oxidase inhibitor program (led by ME-143, with first-gen Phenoxodiol) and the mitochondrial inhibitor program (led by ME-344, with first-gen NV-128). The platform has generated over 400 synthetic compounds based on naturally-occurring plant isoflavones.

Product and service5 records
1ME-143
Categorydrug_candidate
Description

Next-generation NADH oxidase inhibitor and primary active metabolite of Triphendiol. Demonstrates superior anti-tumor activity against a broad range of tumor cell lines compared to Phenoxodiol and Triphendiol. FDA IND approved with Phase I clinical trial initiated in September 2011 for patients with refractory solid tumors.

2ME-344
Categorydrug_candidate
Description

Next-generation mitochondrial inhibitor and active metabolite of NV-128, showing tenfold more anti-tumor activity than NV-128 in pre-clinical studies. Targets the terminal respiratory chain complex in rapidly proliferating cells and induces caspase-independent cell death. IND application submitted in Q1 2012.

3Phenoxodiol
Categorydrug_candidate
Description

First-generation NADH oxidase inhibitor that has been well tolerated in hundreds of patients. Administered via oral or intravenous routes in multiple clinical trials including the Phase III OVATURE trial.

4NV-128
Categorydrug_candidate
Description

First-generation mitochondrial inhibitor that induces caspase-independent cell death through both DNA fragmentation and destructive autophagy, targeting the terminal respiratory chain complex in rapidly proliferating cells.

5Triphendiol (NV-196)
Categorydrug_candidate
Description

Second-generation isoflavone derivative and precursor to ME-143, developed for pancreaticobiliary cancers. Phase Ia clinical trial completed.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Research collaboration with Dr. Gil Mor, gynecological oncologist at Yale School of Medicine, on the mitochondrial inhibitor program. Dr. Mor's research demonstrated NV-128's activity against chemotherapy-resistant ovarian cancer stem cells, leading to identification of next-generation compound ME-344.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage US oncology company developing small molecule therapeutics for solid tumors (notably breast cancer) with similar small-cap, single-platform profile. Both companies operated as thinly-traded Nasdaq-listed clinical biotechs advancing late-Phase I/II assets.

TypeDirect peer
Description

Clinical-stage US oncology company that acquired certain isoflavone-technology assets with ties to the Marshall Edwards/Novogen lineage. Focused on small molecule drug development targeting cancer stem cells and solid tumors with comparable small-cap profile.

3MEI Pharma
TypeDirect peer
Description

Clinical-stage US oncology company with similar size, small-cap Nasdaq profile, and pipeline of small molecule hematologic and solid tumor candidates. Directly comparable as a near-pure-play clinical-stage oncology biotech of the same era.

TypeDirect peer
Description

Clinical-stage US oncology company focused on small molecule kinase inhibitor discovery (later acquired by Merck). Directly comparable as a small-cap, Nasdaq-listed clinical-stage oncology biotech of the same era with a similar pipeline-stage profile.

TypeDirect peer
Description

Clinical-stage US oncology biotech of similar size developing small molecule telomerase-targeted therapy (imetelstat) for hematologic malignancies. Comparable as a small-cap, Nasdaq-listed clinical oncology company with a single-platform, mechanism-focused pipeline.

TypeDirect peer
Description

Clinical-stage US oncology company developing small molecule therapeutics for solid tumors and hematologic malignancies (PI3K/mTOR pipeline). Comparable stage, scale, and focus on novel mechanism oncology drug development.

TypeDirect peer
Description

Clinical-stage biotech developing engineered toxin-based oncology candidates and small molecule therapeutics (formerly Threshold Pharmaceuticals before merger). Comparable as a small-cap clinical-stage oncology company with platform-derived candidates targeting solid tumor metabolism.

TypeDirect peer
Description

Clinical-stage US oncology company developing small molecule targeted therapeutics against solid tumors during a similar time period. Closely matches Marshall Edwards' stage, capitalization profile, and focus on tumor metabolism/DNA-damage pathways.

TypeDirect peer
Description

Clinical-stage US oncology company developing small molecule kinase inhibitors for hematologic malignancies. Directly comparable as a thinly-traded, small-cap, Nasdaq-listed clinical oncology biotech advancing novel-mechanism candidates in the same era.

TypeDirect peer
Description

Australian oncology biotech and majority shareholder/parent of Marshall Edwards; originally developed the isoflavone platform that ME-143 and ME-344 were derived from. Operates in the same therapeutic area with overlapping mechanistic lineage, making it the most directly comparable peer.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Marshall Edwards, Inc.

Oncology Therapeuticsmarshalledwardsinc.com

Marshall Edwards, Inc. is a San Diego-based clinical-stage oncology company developing isoflavone-based anti-cancer therapeutics, with lead candidates ME-143 (NADH oxidase inhibitor in Phase I) and ME-344 (mitochondrial inhibitor) targeting chemotherapy-resistant solid tumors for eventual out-licensing to pharmaceutical partners.

What Marshall Edwards, Inc. does

Marshall Edwards, Inc. is a clinical-stage oncology company headquartered in San Diego, California, that develops novel anti-cancer therapeutics derived from an isoflavone-based chemistry platform originally licensed from its majority shareholder and Australian parent, Novogen Limited (ASX:NRT). The company was incorporated in Delaware in December 2000, began trading on Nasdaq (ticker: MSHL) in December 2003, and relocated its headquarters from Sydney to San Diego in April 2010 following the appointment of Dr. Daniel Gold as CEO. The lead pipeline is organized around two complementary mechanisms targeting tumor cell metabolism: the NADH oxidase inhibitor program (lead candidate ME-143, with first-generation Phenoxodiol and Triphendiol precursors) and the mitochondrial inhibitor program (lead candidate ME-344, with first-generation NV-128 precursor). The platform has generated more than 400 synthetic chemical structures based on naturally-occurring plant isoflavones, and the company holds exclusive worldwide rights through an IP portfolio of 11 issued U.S. patents, 40+ foreign patents, and 80+ foreign applications acquired from Novogen in May 2011.

The core technology targets cancer cell metabolism through two distinct pathways — ME-143 inhibits the sphingosine kinase-Akt signaling pathway to induce caspase-mediated apoptosis, while ME-344 induces caspase-independent cell death via DNA fragmentation and destructive autophagy by targeting the terminal respiratory chain complex. ME-143 entered a Phase I clinical trial in September 2011 for patients with refractory solid tumors, and ME-344 demonstrated tenfold greater anti-tumor activity than NV-128 in preclinical studies, with an IND application filed in Q1 2012. Marshall Edwards is a pre-revenue, publicly traded development-stage company with 11–50 employees, no commercial products, and no product pricing. Its stated go-to-market is the completion of early-stage clinical trials followed by out-licensing or partnering with pharmaceutical companies for late-stage development and commercialization; its primary customers, when commercial, will be oncology healthcare institutions and patients with chemotherapy-resistant cancers including platinum/taxane-refractory ovarian cancer, KRAS-mutant NSCLC, and prostate cancer. Capital to date has been sourced primarily through a December 2011 $2 million private placement from Novogen Limited, supplemented by periodic equity offerings to fund ongoing R&D and clinical operations.

Marshall Edwards, Inc. firmographics

Firmographics
Name
Marshall Edwards, Inc.
Legal name
Marshall Edwards, Inc.
Website
https://marshalledwardsinc.com
Company type
Public
Founded year
2000
Operating status
Operating
Headcount range
11–50 employees
Short description
Marshall Edwards, Inc. is a San Diego-based clinical-stage oncology company developing isoflavone-based anti-cancer therapeutics, with lead candidates ME-143 (NADH oxidase inhibitor in Phase I) and ME-344 (mitochondrial inhibitor) targeting chemotherapy-resistant solid tumors for eventual out-licensing to pharmaceutical partners.
Ownership category
akta.pro rank

Where Marshall Edwards, Inc. is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Marshall Edwards, Inc. business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales

Revenue model

  1. Private Placement Financing: The company raises capital through private placement offerings. In December 2011, the company sold approximately 1.94 million shares of common stock to its majority shareholder Novogen Limited for gross proceeds of $2 million.
  2. Future Product Revenue: Pre-revenue clinical stage company planning to commercialize drug candidates through partnering agreements with pharmaceutical companies upon successful clinical development and regulatory approval.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Marshall Edwards, Inc. product offering

Product offering

Core offering

Marshall Edwards, Inc. is a clinical-stage oncology company developing novel anti-cancer therapeutics based on an isoflavone technology platform derived from naturally occurring plant compounds. The company's lead programs focus on two families of small molecules that target tumor cell metabolism: the NADH oxidase inhibitor program led by ME-143, and the mitochondrial inhibitor program led by ME-344, supported by first-generation compounds Phenoxodiol, NV-128, and Triphendiol.

Product overview

Marshall Edwards is a San Diego-based oncology company developing a pipeline of novel anti-cancer therapeutics derived from an isoflavone technology platform. The company's lead programs focus on two families of small molecules targeting tumor cell metabolism: the NADH oxidase inhibitor program (led by ME-143, with first-gen Phenoxodiol) and the mitochondrial inhibitor program (led by ME-344, with first-gen NV-128). The platform has generated over 400 synthetic compounds based on naturally-occurring plant isoflavones.

Differentiator

Problem solved

Functional benefit

Products and services

  • ME-143 Next-generation NADH oxidase inhibitor and primary active metabolite of Triphendiol. Demonstrates superior anti-tumor activity against a broad range of tumor cell lines compared to Phenoxodiol and Triphendiol. FDA IND approved with Phase I clinical trial initiated in September 2011 for patients with refractory solid tumors.
  • ME-344 Next-generation mitochondrial inhibitor and active metabolite of NV-128, showing tenfold more anti-tumor activity than NV-128 in pre-clinical studies. Targets the terminal respiratory chain complex in rapidly proliferating cells and induces caspase-independent cell death. IND application submitted in Q1 2012.
  • Phenoxodiol First-generation NADH oxidase inhibitor that has been well tolerated in hundreds of patients. Administered via oral or intravenous routes in multiple clinical trials including the Phase III OVATURE trial.
  • NV-128 First-generation mitochondrial inhibitor that induces caspase-independent cell death through both DNA fragmentation and destructive autophagy, targeting the terminal respiratory chain complex in rapidly proliferating cells.
  • Triphendiol (NV-196) Second-generation isoflavone derivative and precursor to ME-143, developed for pancreaticobiliary cancers. Phase Ia clinical trial completed.

Quantifiable outcome

  • ME-143 demonstrated superior anti-tumor activity against a broad range of tumor cell lines compared to Phenoxodiol and Triphendiol in pre-clinical studies
  • +2 more outcomes

Companies that use Marshall Edwards, Inc.

Customer profile

Segments2 records

Ideal customer profiles3 records

Marshall Edwards, Inc. technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Marshall Edwards, Inc. partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Yale University School of Medicine (Dr. Gil Mor)coreStrategic or Co-development PartnerResearch collaboration with Dr. Gil Mor, gynecological oncologist at Yale School of Medicine, on the mitochondrial inhibitor program. Dr. Mor's research demonstrated NV-128's activity against chemotherapy-resistant ovarian cancer stem cells, leading to identification of next-generation compound ME-344.

Scale indicators3 records

Recent moves8 records

Expansion highlights4 records

Marshall Edwards, Inc. competitors and assessment

Company assessment

Direct peers

  • Puma Biotechnology: Clinical-stage US oncology company developing small molecule therapeutics for solid tumors (notably breast cancer) with similar small-cap, single-platform profile. Both companies operated as thinly-traded Nasdaq-listed clinical biotechs advancing late-Phase I/II assets.
  • Verastem: Clinical-stage US oncology company that acquired certain isoflavone-technology assets with ties to the Marshall Edwards/Novogen lineage. Focused on small molecule drug development targeting cancer stem cells and solid tumors with comparable small-cap profile.
  • MEI Pharma: Clinical-stage US oncology company with similar size, small-cap Nasdaq profile, and pipeline of small molecule hematologic and solid tumor candidates. Directly comparable as a near-pure-play clinical-stage oncology biotech of the same era.
  • ArQule: Clinical-stage US oncology company focused on small molecule kinase inhibitor discovery (later acquired by Merck). Directly comparable as a small-cap, Nasdaq-listed clinical-stage oncology biotech of the same era with a similar pipeline-stage profile.
  • Geron Corporation: Clinical-stage US oncology biotech of similar size developing small molecule telomerase-targeted therapy (imetelstat) for hematologic malignancies. Comparable as a small-cap, Nasdaq-listed clinical oncology company with a single-platform, mechanism-focused pipeline.
  • Infinity Pharmaceuticals: Clinical-stage US oncology company developing small molecule therapeutics for solid tumors and hematologic malignancies (PI3K/mTOR pipeline). Comparable stage, scale, and focus on novel mechanism oncology drug development.
  • Molecular Templates: Clinical-stage biotech developing engineered toxin-based oncology candidates and small molecule therapeutics (formerly Threshold Pharmaceuticals before merger). Comparable as a small-cap clinical-stage oncology company with platform-derived candidates targeting solid tumor metabolism.
  • Clovis Oncology: Clinical-stage US oncology company developing small molecule targeted therapeutics against solid tumors during a similar time period. Closely matches Marshall Edwards' stage, capitalization profile, and focus on tumor metabolism/DNA-damage pathways.
  • Sunesis Pharmaceuticals: Clinical-stage US oncology company developing small molecule kinase inhibitors for hematologic malignancies. Directly comparable as a thinly-traded, small-cap, Nasdaq-listed clinical oncology biotech advancing novel-mechanism candidates in the same era.
  • Novogen Limited: Australian oncology biotech and majority shareholder/parent of Marshall Edwards; originally developed the isoflavone platform that ME-143 and ME-344 were derived from. Operates in the same therapeutic area with overlapping mechanistic lineage, making it the most directly comparable peer.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Marshall Edwards, Inc. financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Marshall Edwards, Inc. leadership team

Management profile

Number of profiles

Profiles2 records

Marshall Edwards, Inc. funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Marshall Edwards, Inc. M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Marshall Edwards, Inc.

What does Marshall Edwards, Inc. do?

Marshall Edwards, Inc. is a clinical-stage oncology company developing novel anti-cancer therapeutics based on an isoflavone technology platform derived from naturally occurring plant compounds. The company's lead programs focus on two families of small molecules that target tumor cell metabolism: the NADH oxidase inhibitor program led by ME-143, and the mitochondrial inhibitor program led by ME-344, supported by first-generation compounds Phenoxodiol, NV-128, and Triphendiol.

Is Marshall Edwards, Inc. a public or private company?

Marshall Edwards, Inc. is a public company. It is classified as corporate owned and is currently operating.

When was Marshall Edwards, Inc. founded?

Marshall Edwards, Inc. was founded in 2000. It employs 11 to 50 people.

Where is Marshall Edwards, Inc. based?

Marshall Edwards, Inc. is headquartered in San Diego, United States, in the North America region.

How does Marshall Edwards, Inc. make money?

Two revenue lines are on record. Private Placement Financing is the primary driver. The others are future Product Revenue.

Who are Marshall Edwards, Inc.'s main competitors?

Direct peers on record are Puma Biotechnology, Verastem, MEI Pharma, ArQule, Geron Corporation, Infinity Pharmaceuticals, Molecular Templates, Clovis Oncology, Sunesis Pharmaceuticals and Novogen Limited.

Does Marshall Edwards, Inc. have an API?

No public API is recorded for Marshall Edwards, Inc..

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Live signals
GlobeNewswireMarshall Edwards, Inc. Receives Nasdaq Notice of Minimum Stockholders' Equity Non-ComplianceMarshall Edwards, Inc. received a Nasdaq notice on May 18, 2010, that its stockholders' equity of $9.16 million fell below the $10 million minimum for Nasdaq Global Market listing. The company has 45 days to submit a compliance plan, with an optional 180-day extension, and may seek a capital raise or transfer to the Nasdaq Capital Market.GlobeNewswireMarshall Edwards, Inc. Announces Grants Under Nasdaq Rule 5635Marshall Edwards granted non-qualified stock options to CEO Daniel P. Gold for 220,390 shares in two tranches. The first tranche vested 25% one year after appointment, with the remaining 75% vesting monthly over 36 months, and full vesting upon a change in control.GlobeNewswireMarshall Edwards, Inc. Receives Nasdaq Staff DeterminationMarshall Edwards, Inc. received a Nasdaq staff determination on March 16, 2010, that its stock is subject to delisting on March 25, 2010, for failing to meet the $1.00 minimum bid price. The company plans to request a hearing on March 23, 2010, and has approved a reverse stock split pending stockholder approval on March 29, 2010.GlobeNewswireMarshall Edwards, Inc.'s Action Intended to Regain Compliance With Nasdaq Share Price Rule, Benefit ShareholdersMarshall Edwards, Inc. announced its board approved a 1-for-10 reverse stock split to regain Nasdaq share price compliance. The split is subject to stockholder approval, with a special meeting planned for March 2010. The company has until March 15, 2010, to meet Nasdaq's $1.00 share price standard.GlobeNewswireMarshall Edwards, Inc. Announces Resignation of Christopher Naughton From Board of DirectorsMarshall Edwards, Inc. announced that Christopher Naughton resigned as a board member effective February 5, 2010. The board's size decreased from five to four members, and the company intends to fill the vacancy.GlobeNewswireMarshall Edwards, Inc.'s NV-128, a Novel mTOR Inhibitor, Demonstrates Good Safety Profile and High Anti-Cancer Activity In VivoMarshall Edwards released data on NV-128, an mTOR inhibitor, showing tumor volume reduction of 51% in mice with ovarian cancer xenografts after 15 days, with weight gain versus rapamycin's weight loss. The compound also showed no cardiac toxicity, and the company plans to seek approval for human clinical trials.GlobeNewswireIndependent Data Monitoring Committee Reviews Marshall Edwards, Inc.'s Arrangements for Data Analysis of the Ovature TrialThe Independent Data Monitoring Committee reviewed data from 117 subjects and supported Marshall Edwards' decision to close the OVATURE trial to accrual after 142 patients were randomized. The committee found no safety concerns with phenoxodiol and recommended final analyses be completed as soon as possible.GlobeNewswireBiotech Analyst Joins Board of Directors of Marshall Edwards, Inc.Marshall Edwards appointed Leah Cann to its board of directors, where she will chair the audit committee. The company also announced that William Rueckert resigned from the board and accepted a position on Novogen's board. Cann brings a background in biotechnology and cancer research.GlobeNewswireMarshall Edwards, Inc. Granted IND for TriphendiolMarshall Edwards, Inc. received FDA IND approval to study triphendiol with gemcitabine in pancreatic and bile duct cancers. The approval enables a Phase Ib study in unresectable, locally advanced, or metastatic patients. Triphendiol holds orphan drug status for these indications.