Molecular Templates, Inc. Reports Third Quarter 2018 Financial Results and Provides Corporate Update
“Our recently announced CD38 collaboration with Takeda enables the development of TAK-169, the most potent ETB we have created with our platform to date. Importantly, the upfront payment from Takeda and the equity financing that we closed in September provide the funding to allow us to generate clinical data from multiple pipeline candidates throughout 2019 and beyond,” said
Company Highlights and Upcoming Milestones
September 19, 2018, Molecular announced an agreement with Takeda for the joint development of CD38-targeted ETBs for the treatment of multiple myeloma. TAK-169, the lead development candidate, is a CD38-targeted ETB that resulted from a previous discovery collaboration between the two companies. Under the terms of the agreement, Takeda made an upfront payment of $30 millionand Molecular is eligible to receive development, regulatory and commercial milestone payments of up to $632.5 millionif Molecular exercises its co-development option or $337.5 millionif Molecular does not exercise or opts out of its co-development option. Takeda has also agreed to pay royalties on the sales of the commercial products developed through the collaboration. The royalty percentages would range from low double-digits to low twenties if Molecular exercises its option to co-develop, and from high-single digits to low teens if Molecular does not exercise its option to co-develop. Molecular and Takeda will share equally in the development costs.
September 18, 2018, Molecular entered into a Cancer Research Grant Contractwith the Cancer Prevention and Research Institute of Texas(CPRIT), in connection with a grant of approximately $15.2 millionawarded by CPRIT to Molecular in November 2016to fund research of a cancer therapy involving a CD38 targeting ETB (MT-4019). Molecular may also use such funds to develop a replacement CD38 targeting ETB, with or without a partner and expects to use this grant to fund development of TAK-169.
September 25, 2018, Molecular announced the closing of an underwritten public offering of its common stock, which generated gross proceeds of approximately $52 million.
- Following the announcement of the CD38 joint development agreement in September, Takeda and Molecular are conducting IND enabling studies for TAK-169, which is expected to enter the clinic for the treatment of multiple myeloma in 2019.
- Molecular expects to begin enrollment in 4Q18 for a Phase II combination study with MT-3724 and chemotherapy in earlier lines of diffuse large B-cell lymphoma (DLBCL).
- In 1Q19 Molecular expects to start a Phase II monotherapy study, which has the potential to be a pivotal study.
- Molecular expects to initiate a second Phase II combination study with MT-3724 and Revlimid® (lenalidomide) in earlier lines of DLBCL in 1Q19.
- Molecular expects to file an IND application for an ETB targeting HER2 in 1Q19.
- Molecular expects to file an IND application for an ETB targeting PD-L1 (with antigen seeding) in 2H19.
- Several other ETB candidates are in pre-clinical development, targeting both solid and hematological cancers.
Takeda Multi-Target Collaboration
- Takeda and Molecular are conducting lead optimization for ETBs against two undisclosed targets selected by Takeda under the collaboration. Should Takeda exercise its option to license ETBs for both targets, Molecular would receive
$25 millionand would be eligible to receive up to $547 millionin milestone payments and tiered royalties on sales.
The net loss attributable to common shareholders for the third quarter of 2018 was $5.2 million, or
Revenues for the third quarter of 2018 were $6.8 million, compared to
The net loss attributable to common shareholders for the nine months ended
Revenues for the nine months ended
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 share and per share data)
Three Months Ended
Nine Months Ended
|Research and development revenue||$||2,031||$||648||$||3,206||$||2,408|
|Research and development||8,290||2,522||22,640||4,829|
|General and administrative||3,538||3,996||10,165||8,233|
|Total operating expenses||11,828||6,518||32,805||13,062|
|Loss from operations||5,076||5,870||24,204||10,487|
|Interest and other income, net||107||1||307||2|
|Change in fair value of warrant liabilities||4||(272||)||916||(269||)|
|Loss on conversion of notes||—||(4,719||)||—||(4,719||)|
|Deemed dividends on preferred stock||—||(138||)||—||(958||)|
|Net loss attributable to common shareholders||$||5,244||$||11,105||$||23,653||$||17,183|
|Net loss per share attributable to common shareholders:|
|Basic and diluted||$||0.19||$||0.62||$||0.87||$||2.75|
|Weighted average number of shares used in net loss per share calculations:|
|Basic and diluted||27,680,307||17,925,585||27,246,667||6,241,947|
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands, except share and per share data)
|Cash and cash equivalents||$||78,744||$||58,910|
|Accounts receivable from related party||31,163||—|
|Other current assets||4,385||19|
|Total current assets||116,827||60,414|
|Property and equipment, net||7,165||1,952|
|In-process research and development||26,623||26,623|
|LIABILITIES AND STOCKHOLDERS’ EQUITY|
|Current portion of long-term debt||—||2,400|
|Other current liabilities||106||70|
|Total current liabilities||41,731||10,442|
|Long-term debt, net||3,155||1,078|
|Total stockholders’ equity||106,192||77,289|
|Total liabilities and stockholders’ equity||$||151,960||$||90,391|
Source: Molecular Templates, Inc.