MEI Pharma Reports Third Quarter Fiscal Year 2024 Results and Operational Highlights
MEI Pharma, a clinical-stage pharmaceutical company, reported positive results for the third quarter fiscal year 2024, highlighting promising clinical data for voruciclib and ME-344. The ongoing Phase 1 study evaluating voruciclib plus venetoclax in R/R AML patients showed anti-leukemic activity, with complete responses and significant decreases in Mcl-1 levels. MEI's Board of Directors is focused on advancing the voruciclib program, with a cash balance of $56.6 million. MEI also initiated research on a new ME-344 formulation and decided to prioritize clinical development of voruciclib. Financially, MEI had no debt, $56.6 million in cash, and believes its cash balance is sufficient for the next 12 months.
Positive results from the ongoing Phase 1 study evaluating voruciclib plus venetoclax in R/R AML patients, showing anti-leukemic activity, complete responses, and decreases in Mcl-1 levels.
MEI's Board of Directors unanimously aligned on prioritizing the clinical development of voruciclib, highlighting confidence in the drug's potential.
MEI reported a cash balance of $56.6 million with no outstanding debt, ensuring financial stability and operational sustainability.
No revenue was recognized for the quarter ended March 31, 2024, compared to $5.9 million for the same period in 2023, impacting the company's financial performance.
Cash used in operations for the nine months ended March 31, 2024, amounted to $32.5 million, compared to $41.2 million in the previous year, indicating a significant cash burn rate.
Research and development expenses decreased by $9.9 million to $5.2 million for the quarter ended March 31, 2024, possibly affecting future drug development activities.
Insights
-- Ongoing Phase 1 Study Evaluating Voruciclib Plus Venetoclax Demonstrates Anti-leukemic Activity, Including Complete Responses, Anticipated Decreases in Mcl-1 and No Overlapping Toxicity in Heavily Pretreated R/R AML Patients --
-- Board of Directors Unanimously Aligned on Prioritization of Voruciclib Program Development--
-- MEI Begins Fourth Fiscal Quarter with
“Over the past several months, MEI has received encouraging clinical data for voruciclib and ME-344 supporting the further development of these programs,” said David Urso, president and chief executive officer of MEI Pharma. “The clinical focus for the rest of the year will be voruciclib, our oral CDK9 inhibitor. We anticipate providing updates from the clinical trial evaluating voruciclib in combination with venetoclax in patients with relapsed/refractory AML, a study designed to provide additional evidence of the anti-leukemic activity of this combination, during the remainder of calendar 2024.”
Mr. Urso continued: “While venetoclax is an established option for patients with AML and is increasingly used as a standard treatment, the disease typically progresses and patients require therapy after venetoclax, which consistently yields limited benefit. While treatments targeting specific patient populations with mutations such as FLT3 and IDH and the menin inhibitors may be an option for some relapsed/refractory AML patients, the majority of patients do not have therapeutically actionable mutations. We believe that voruciclib in combination with venetoclax has potential, as a mutation-agnostic therapy, to benefit the largest number of patients with relapsed/refractory AML.”
Select Third Quarter Fiscal Year 2024 and Recent Highlights
- In January 2024, MEI presented a Trials in Progress poster of the Phase 1b study of ME-344, an investigational inhibitor of mitochondrial oxidative phosphorylation (“OXPHOS”), evaluating the combination with bevacizumab (Avastin®) in refractory metastatic colorectal cancer patients at the 2024 ASCO Gastrointestinal Cancers Symposium.
- In March 2024, MEI reported initiation of enrollment in an expansion cohort in the ongoing Phase 1 study evaluating voruciclib, its investigational selective oral cyclin-dependent kinase 9 (“CDK9”) inhibitor, in combination with venetoclax (Venclexta®), a B-cell lymphoma 2 (“BCL2”) inhibitor, in relapsed and refractory (“R/R”) acute myeloid leukemia (“AML”) patients. The decision to open the expansion cohort was based on initial data demonstrating anti-leukemic activity, including complete responses in heavily pretreated patients. Additionally, at doses of 100 mg or more, initial results from correlative biomarker assay analyses of available samples from patients treated with the combination demonstrated anticipated decreases of myeloid leukemia cell differentiation protein (“Mcl-1”), including progressively greater decreases in Mcl-1 in patients achieving a response compared to patients with stable disease or progressive disease. We also observed expected increases in Mcl-1 after administering venetoclax and subsequent anticipated decreases in Mcl-1 after administering voruciclib, supporting our hypothesis that voruciclib, as an inhibitor of CDK9, regulates Mcl-1 and therefore may address the increase of Mcl-1 levels associated with venetoclax. There was no evidence of overlapping toxicity with venetoclax and no dose limiting toxicities were observed.
-
In April 2024, MEI reported that
25% of evaluable patients with relapsed metastatic colorectal cancer in Cohort 1 of the Phase 1b study evaluating ME-344, an investigational inhibitor of mitochondrial oxidative phosphorylation, in combination with bevacizumab (Avastin®) had no disease progression at Week 16. This landmark analysis exceeded the20% threshold set in the Clinical Study Protocol to add an additional 20 patients to the study via the initiation of Cohort 2. The combination was also observed to be generally well-tolerated to date. While the threshold was met to proceed to Cohort 2, following a strategic review the Company decided to continue to advance ME-344 via its ongoing development of a new formulation rather than through the addition of a new cohort of patients. The Company has already initiated research and development activity of the new formulation with the goal of increasing biological activity, improving convenience of administration and increasing the commercial opportunity.
- In April 2024, MEI reported that its Board of Directors unanimously aligned on a strategy to prioritize clinical development of voruciclib and enable development of a new ME-344 formulation for the potential of a future Phase 1 study. Additionally, the Company’s Board of Directors unanimously determined not to proceed with a second return of capital under the October 31, 2023, Anson Funds and Cable Car Capital cooperation agreement in order to conserve resources and align strategic investment, and thereby extend the Company’s operational cash runway.
Expected Drug Candidate Pipeline Developments
Voruciclib – Oral CDK9 inhibitor in Phase 1 Study
-
MEI expects to report clinical data from additional dose escalation and expansion cohorts of the ongoing Phase 1 clinical trial evaluating voruciclib plus venetoclax in patients with R/R AML during the remainder of calendar 2024.
The Company has completed patient enrollment of the dose expansion cohort evaluating a 300 mg dose of voruciclib administered daily for 14 consecutive days in a 28-day cycle in combination with standard dose venetoclax. Additionally, MEI is enrolling dose escalation cohorts evaluating up to four dose levels of voruciclib starting at 150 mg administered daily for 21 consecutive days in a 28-day cycle in combination with venetoclax.
ME-344 –Inhibitor of Mitochondrial OXPHOS in Phase 1b Study
- MEI has initiated research and development activity of a new ME-344 formulation with the goal of increasing biological activity, improving convenience of administration and increasing the commercial opportunity. The Company expects to provide an update on our formulation efforts in the first half of calendar 2025.
Select Third Quarter and Nine Months Financial Results for Fiscal Year 2024
-
As of March 31, 2024, MEI had
$56.6 million
-
For the nine months ended March 31, 2024, cash used in operations was
$32.5 million $41.2 million
-
Research and development expenses decreased by
$9.9 million $5.2 million $15.1 million
-
General and administrative expenses decreased by
$2.6 million $4.6 million $7.2 million
-
MEI recognized no revenue for the quarter ended March 31, 2024, compared to
$5.9 million
The Company believes its cash balance is sufficient to fund operations for at least the next 12 months.
About MEI Pharma
MEI Pharma, Inc. (Nasdaq: MEIP) is a clinical-stage pharmaceutical company committed to developing novel and differentiated cancer therapies. We build our pipeline by acquiring promising cancer agents and creating value in programs through development, strategic partnerships, out-licensing and commercialization, as appropriate. Our approach to oncology drug development is to evaluate our drug candidates in combinations with standard-of-care therapies to overcome known resistance mechanisms and address clear medical needs to provide improved patient benefit. The drug candidate pipeline includes voruciclib, an oral cyclin-dependent kinase 9 ("CDK9") inhibitor, and ME-344, an intravenous small molecule inhibitor of mitochondrial oxidative phosphorylation. For more information, please visit www.meipharma.com. Follow us on X (formerly Twitter) @MEI_Pharma and on LinkedIn.
Forward-Looking Statements
Certain information contained in this press release that are not historical in nature are “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, Section 21E of the Securities Exchange Act of 1934, as amended, and the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, including, without limitation, statements regarding: the potential, safety, efficacy, and regulatory and clinical progress of our product candidates, including the anticipated timing for initiation of clinical trials and release of clinical trial data and our expectations surrounding potential regulatory submissions, approvals and timing thereof, our business strategy and plans; our future financial position, including the sufficiency of our cash, cash equivalents and short-term investments to fund our operations and our ability to fund future capital returns; and the objectives of management for future operations. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management’s current expectations and projections about future events. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including, but not limited to our failure to successfully commercialize our product candidates; the availability or appropriateness of utilizing the FDA’s accelerated approval pathway for our product candidates; final data from our pre-clinical studies and completed clinical trials may differ materially from reported interim data from ongoing studies and trials; costs and delays in the development and/or FDA approval, or the failure to obtain such approval, of our product candidates; uncertainties or differences in interpretation in clinical trial results; uncertainty regarding the impact of rising inflation and the increase in interest rates as a result; potential economic downturn; geopolitical conflicts; activist investors; our inability to maintain or enter into, and the risks resulting from, our dependence upon collaboration or contractual arrangements necessary for the development, manufacture, commercialization, marketing, sales and distribution of any products; competitive factors; our inability to protect our patents or proprietary rights and obtain necessary rights to third party patents and intellectual property to operate our business; our inability to operate our business without infringing the patents and proprietary rights of others; general economic conditions; the failure of any products to gain market acceptance; our inability to obtain any additional required financing; technological changes; government regulation; changes in industry practice; and one-time events. We do not intend to update any of these factors or to publicly announce the results of any revisions to these forward-looking statements. Under
MEI Pharma, Inc. |
||||||||
Condensed Consolidated Balance Sheets |
||||||||
(in thousands, except par value amounts) |
||||||||
|
|
March 31,
|
|
June 30,
|
||||
|
|
(Unaudited) |
|
(Audited) |
||||
ASSETS |
||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ |
2,368 |
|
$ |
16,906 |
|
||
| Short-term investments |
|
54,184 |
|
|
83,787 |
|
||
| Unbilled receivables |
|
— |
|
|
85 |
|
||
| Prepaid expenses and other current assets |
|
2,814 |
|
|
6,750 |
|
||
| Total current assets |
|
59,366 |
|
|
107,528 |
|
||
| Operating lease right-of-use asset |
|
10,836 |
|
|
11,972 |
|
||
| Property and equipment, net |
|
1,058 |
|
|
1,309 |
|
||
| Total assets | $ |
71,260 |
|
$ |
120,809 |
|
||
LIABILITIES AND STOCKHOLDERS’ EQUITY |
||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ |
3,176 |
|
$ |
6,134 |
|
||
| Accrued liabilities |
|
5,388 |
|
|
12,461 |
|
||
| Deferred revenue |
|
— |
|
|
317 |
|
||
| Operating lease liability |
|
1,052 |
|
|
1,428 |
|
||
| Total current liabilities |
|
9,616 |
|
|
20,340 |
|
||
| Deferred revenue, long-term |
|
— |
|
|
64,545 |
|
||
| Operating lease liability, long-term |
|
10,615 |
|
|
11,300 |
|
||
| Total liabilities |
|
20,231 |
|
|
96,185 |
|
||
| Commitments and contingencies | ||||||||
| Stockholders’ equity: | ||||||||
| Preferred stock, |
|
— |
|
|
— |
|
||
| Common stock, |
|
— |
|
|
— |
|
||
| Additional paid-in capital |
|
420,842 |
|
|
430,621 |
|
||
| Accumulated deficit |
|
(369,813 |
) |
|
(405,997 |
) |
||
| Total stockholders’ equity |
|
51,029 |
|
|
24,624 |
|
||
| Total liabilities and stockholders’ equity | $ |
71,260 |
|
$ |
120,809 |
|
||
MEI Pharma, Inc. |
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Condensed Consolidated Statements of Operations |
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(Unaudited) |
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(in thousands, except per share amounts) |
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|
|
|
|
|
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|
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Three Months Ended
|
|
Nine Months Ended
|
||||||||||||
|
|
2024 |
|
2023 |
|
2024 |
|
2023 |
||||||||
| Revenues | $ |
— |
|
$ |
5,894 |
|
$ |
65,297 |
|
$ |
47,359 |
|
||||
| Operating expenses: | ||||||||||||||||
| Research and development |
|
5,220 |
|
|
15,104 |
|
|
12,617 |
|
|
49,880 |
|
||||
| General and administrative |
|
4,609 |
|
|
7,181 |
|
|
19,158 |
|
|
23,163 |
|
||||
| Total operating expenses |
|
9,829 |
|
|
22,285 |
|
|
31,775 |
|
|
73,043 |
|
||||
| (Loss) income from operations |
|
(9,829 |
) |
|
(16,391 |
) |
|
33,522 |
|
|
(25,684 |
) |
||||
| Other income (expense): | ||||||||||||||||
| Change in fair value of warrant liability |
|
— |
|
|
— |
|
|
— |
|
|
1,603 |
|
||||
| Interest and dividend income |
|
706 |
|
|
957 |
|
|
2,669 |
|
|
2,282 |
|
||||
| Other expense, net |
|
(4 |
) |
|
(4 |
) |
|
(7 |
) |
|
(10 |
) |
||||
| Net (loss) income | $ |
(9,127 |
) |
$ |
(15,438 |
) |
$ |
36,184 |
|
$ |
(21,809 |
) |
||||
| Net (loss) income per share - basic and diluted | $ |
(1.37 |
) |
$ |
(2.32 |
) |
$ |
5.43 |
|
$ |
(3.27 |
) |
||||
| Weighted-average shares used in computing net (loss) income per share - basic and diluted: |
|
6,663 |
|
|
6,663 |
|
|
6,663 |
|
|
6,663 |
|
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View source version on businesswire.com: https://www.businesswire.com/news/home/20240509996400/en/
David A. Walsey
MEI Pharma
Tel: 858-369-7104
investor@meipharma.com
Source: MEI Pharma, Inc.
FAQ
What positive results were reported by MEI Pharma for the third quarter fiscal year 2024?
What is the cash balance of MEI Pharma as of March 31, 2024?
What drug candidates are MEI Pharma focusing on in its pipeline developments?
