Molecular Templates, Inc. Reports Fourth Quarter 2017 Financial Results
Update on MT-3724 Provided at
Upcoming Presentations at
“We are excited by the continued progress of our pipeline as well as our partnership with Takeda,” said
Company Highlights and Upcoming Milestones
- In 4Q17, Molecular expanded its senior management team with the additions of
Adam Cutleras Chief Financial Officer; Barbara Ruskin J.D. Ph.D. as SVP, General Counsel and Chief Patent Officer; Nenad Sarapa M.D. M.S. as SVP of Clinical Development, and Conrad Jordaanas SVP of Finance and Corporate Controller.
March 2, 2018, Molecular closed a $10 milliondebt facility with Perceptive Advisors. The proceeds were used to repay an existing debt facility with Silicon Valley Bankand will support Molecular’s build out of its GMP manufacturing facility, which should shorten the time from lead development to IND and better support Molecular’s own pipeline as well as partnerships.
- MT-3724 (an ETB targeting CD20) is in an ongoing Phase Ib expansion study intended to better define the overall response rate to this candidate as a single-agent in heavily pre-treated diffuse large B-cell lymphoma (DLBCL) patients.
- A brief update on the first three patients dosed in the MT-3724 Phase Ib expansion study was delivered at the World ADC Summit Europe today. Observations included the following:
- One of the three patients achieved a partial response (PR) after a single dose of MT-3724. The PR was confirmed at the end of cycle 2 per protocol and the patient remains on study with continued dosing of MT-3724. The other two patients were assessed as having stable disease (SD) and progressive disease (PD).
- A dose interruption and reduction was required in two of the first three patients in Phase Ib expansion. These patients had high body weights which resulted in high absolute doses of MT-3724 based on 75 mcg/kg dosing. The adverse events observed (grade 2 and 3) were reversible and dosing resumed at 50 mcg/kg, which has been generally well tolerated.
- Based on these data, the deep and sustained clinical responses to MT-3724 observed at doses as low as 5 mcg/kg, as well as the near-complete peripheral B-cell depletion at doses up to 50 mcg/kg, the maximum tolerated dose (MTD) of MT-3724, has been defined as 50 mcg/kg with a maximum total drug per dose of 6,000 mcg, or 6 mg.
- Enrollment in the Phase Ib expansion study continues, with further updates on results expected in 2Q18.
- Nine DLBCL patients with low serum levels of rituximab have been treated at doses ranging from 5 mcg/kg to 75 mcg/kg in the Phase I dose-finding and Phase Ib expansion studies. In these nine patients, one complete response, two partial responses, three patients with stable disease (including one patient with a 48% reduction in tumor size), and three patients with progressive disease, were observed.
- Based on the peripheral B-cell depletion observed at 50 mcg/kg and responses seen at doses as low as 5 mcg/kg, 50 mcg/kg appears to be an efficacious and well-tolerated dose.
- Molecular also expects to initiate combination studies with MT-3724 in earlier lines of DLBCL therapy in 2Q18.
December 2017, Takeda selected two targets for further research using Molecular’s ETBs. This has triggered $4 millionin milestone payments to be paid by Takeda in 2018.
- Takeda and Molecular are evaluating CD38 ETBs and could select a drug candidate for development by the end of 2Q18.
- MT-4019, an ETB candidate that is designed to target CD38-expressing myeloma cancer cells, is progressing through IND enabling studies. If Takeda and Molecular do not select a joint candidate for development, Molecular anticipates filing an IND application for MT-4019 in mid-2018 to initiate a Phase I clinical trial in
the United Statesin 2H18.
- Preclinical data for Molecular’s ETBs targeting PD-L1 (which incorporates Molecular’s Antigen Seeding Technology – a differentiated immune-oncology approach) and HER2 will be presented at the
American Association of Cancer Research(AACR) annual meeting in April 2018
- Molecular expects to file an IND application for an ETB targeting HER2 in 4Q18
- Molecular expects to file an IND application for an ETB targeting PD-L1 (with antigen seeding) in 1Q19
- Several other ETB candidates are in preclinical development targeting both solid and hematological cancers
The net loss attributable to common shareholders for the fourth quarter was $6.9 million, or $0.26 per basic and diluted share. This is compared to a net loss attributable to common shareholders for the same period in 2016, of $2.9 million, or $13.82 per basic and diluted share.
Revenues for the fourth quarter of 2017 were $0.8 million, compared to
Revenues for the year ended December 31, 2017 were $3.4 million, compared to $1.9 million for 2016. These revenues were primarily comprised of research and development revenues from our collaboration with Takeda of
The net loss attributable to common shareholders for the year ended December 31, 2017 was $24.1 million, or $2.11 per basic and diluted share, compared to a net loss attributable to common shareholders of $12.6 million or $59.04 per basic and diluted share, for 2016. As of December 31, 2017, cash and cash equivalents totaled $58.9 million. Molecular’s current cash balance is expected to fund operations into late 2019.
About Molecular Templates
Molecular Templates is a clinical-stage oncology company focused on the discovery and development of differentiated, targeted, biologic therapeutics for cancer. We believe our proprietary biologic drug platform technology, referred to as engineered toxin bodies, or ETBs, provides a differentiated mechanism of action that may address some of the limitations associated with currently available cancer therapeutics. ETBs utilize a genetically engineered form of Shiga-like Toxin A subunit, or SLTA, a ribosome inactivating bacterial protein, that can be targeted to specifically destroy cancer cells. Additional information about Molecular Templates can be obtained at http://www.mtem.com.
This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the “Act”). Molecular Templates disclaims any intent or obligation to update these forward-looking statements, and claims the protection of the Act’s Safe Harbor for forward-looking statements. All statements, other than statements of historical facts, included in this press release regarding strategy, future operations, future financial position, future revenue, projected expenses, prospects, plans and objectives of management are forward-looking statements. In addition, when or if used in this press release, the words “may,” “could,” “should,” “anticipate,” “believe,” “estimate,” “expect,” “intend,” “plan,” “predict” and similar expressions and their variants, as they relate to Molecular Templates may identify forward-looking statements. Examples of such statements include, but are not limited to, statements relating to the development of the Company’s lead program, MT-3724; the expected timing of submitting various IND applications and initiating studies; and the Company’s belief that its proprietary biologic drug platform technology, or ETBs, provides for a differentiated mechanism of action that may address some of the limitations associated with currently available cancer therapeutics.
Forward-looking statements are not guarantees of future performance and involve risks and uncertainties. Actual events or results may differ materially from those discussed in the forward-looking statements as a result of various factors including, but not limited to, the uncertainties inherent in the preclinical and clinical development process; whether the Company’s cash resources will be sufficient to fund its continuing operations for the periods and/or trials anticipated; the ability of the Company to protect its intellectual property rights; and legislative, regulatory, political and economic developments, as well as those risks identified under the heading “Risk Factors” in the Company’s filings with the
Chief Financial Officer
Condensed Consolidated Statements of Operations
(in thousands, except per share data)
|Three Months Ended||Year Ended|
|December 31,||December 31,||December 31,||December 31,|
|Research and development revenue from collaboration agreements||$||—||$||—||$||2,408||$||—|
|Research and development||4,657||1,658||9,487||8,017|
|General and administrative||3,523||1,110||11,755||4,482|
|Total operating expenses||8,180||2,768||21,242||12,499|
|Interest and other, net||346||(150||)||(674||)||(409||)|
|(Gain)/Loss on conversion of notes||99||—||(4,619||)||—|
|Deemed dividends on preferred stock||—||(393||)||(958||)||(1,572||)|
|Net loss attributable to common shareholders||$||(6,915||)||$||(2,958||)||$||(24,098||)||$||(12,600||)|
|Net loss per share – basic and diluted||$||(0.26||)||$||(13.82||)||$||(2.11||)||$||(59.04||)|
|Weighted average shares used in computing net loss per share – basic and diluted||26,893||214||11,401||213|
Condensed Consolidated Balance Sheets
|December 31,|| December 31,
|Cash and cash equivalents||$||58,910||$||1,716|
|Prepaid expenses and other||1,504||127|
|Total current assets||60,414||1,843|
|Property and equipment, net||1,952||334|
|In-process research and development||26,623||—|
|Intangible assets and other||1,402||921|
|Liabilities and stockholders' equity|
|Accounts payable and accrued liabilities||$||5,207||$||2,144|
|Current portion of long-term debt||2,400||2,400|
|Related party debt||—||7,315|
|Other current liabilities||70||36|
|Total current liabilities||10,442||13,765|
|Long-term debt, net of current portion||1,078||3,165|
|Redeemable convertible preferred stock||25,871|
|Total liabilities and stockholders' equity||$||90,391||$||3,098|
Source: Molecular Templates, Inc.