false
0001485003
0001485003
2023-11-09
2023-11-09
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):
November 9, 2023
Carisma Therapeutics Inc.
(Exact Name of Registrant as Specified in its
Charter)
Delaware |
|
001-36296 |
|
26-2025616 |
(State or other jurisdiction of incorporation) |
|
(Commission File Number) |
|
(IRS Employer Identification No.) |
|
|
|
|
|
3675 Market Street, Suite 200 Philadelphia, PA |
|
|
|
19104 |
(Address of Principal Executive Offices) |
|
|
|
( Zip Code) |
Registrant’s telephone number, including
area code: (267) 491-6422
(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 Section 12(b) of the Act:
|
|
|
|
|
Title of each class |
|
Trading Symbol(s) |
|
Name of exchange on which registered |
Common Stock, $0.001 par value |
|
CARM |
|
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 2.02. Results of Operations and Financial Condition.
On November 9, 2023, Carisma Therapeutics Inc. (the “Company”)
announced its financial results for the quarter ended September 30, 2023. The full text of the press release issued in connection with
the announcement is being furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.
The information in this Item 2.02, including Exhibit 99.1 attached
hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange
Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing made
by the Company under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference
in such a filing.
Item 9.01. Financial Statements and Exhibits.
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.
|
CARISMA THERAPEUTICS INC. |
|
|
|
|
By: |
/s/ Steven Kelly |
Date: November 9, 2023 |
|
Steven Kelly |
|
|
President and Chief Executive Officer |
Exhibit
99.1
Carisma
Therapeutics Reports Third Quarter 2023 Financial Results and Recent Business Highlights
Presented
updated data from Phase 1 clinical trial of CT-0508 at CAR-TCR Summit, further supporting CAR-M safety, feasibility and mechanism of
action
Selected
clinical candidate for CT-1119, an anti-mesothelin CAR-Monocyte
Presented
pre-clinical proof of concept data of in vivo CAR-M, from the Company’s collaboration with Moderna, at SITC
Cash,
cash equivalents and marketable securities of $94.1 million expected to fund company into the first quarter of 2025
PHILADELPHIA
– November 9, 2023 – Carisma Therapeutics Inc. (Nasdaq: CARM) (“Carisma” or the “Company”), a clinical-stage
biopharmaceutical company focused on discovering and developing innovative immunotherapies, today reported financial results for the
quarter ended September 30, 2023, and highlighted recent business updates.
“During
the third quarter, Carisma made several key advancements across our clinical and pre-clinical programs and reported data from both our
Phase 1 clinical study of CT-0508 and our pre-clinical work with Moderna developing in vivo CAR-M,” said Steven Kelly, President
and Chief Executive Officer of Carisma. “We continue to progress CT-0508 and CT-0525, our assets targeting HER2 overexpressing
tumors, as we work to validate our first-in-class engineered macrophage platform. We believe that we have value-driving, next-generation
cell therapies in our pipeline that have the potential to improve the treatments available for patients with cancer and other serious
disorders.”
Third
Quarter 2023 and Recent Business Highlights
| o | Announced
updated data from the Company’s Phase 1 clinical trial of CT-0508, a human epidermal
growth factor receptor 2 (HER2) targeted chimeric antigen receptor macrophage (CAR-M), which
included data from the first five patients from group 2 (single-day bolus dosing). Preliminary
results from the nine patients in group 1 (fractionated dosing) were presented in November
2022. The group 2 data, which were presented at the 8th Annual CAR-TCR Summit,
support primary safety and manufacturing feasibility endpoints of single-day bolus dosing.
The Company believes that translational analyses on early data from the combined groups 1
and 2 show that biomarkers of tumor microenvironment activation, T cell activation, and HER2
status correlate with best overall response of stable disease, providing further evidence
of the CT-0508 mechanism of action. |
| o | Selected
a clinical candidate for the CT-1119 program, a CAR-Monocyte for mesothelin overexpressing
solid tumors. CT-1119 will incorporate two key enhancements: a next-generation CAR that,
as demonstrated in pre-clinical studies, leads to a significant increase in tumor killing
and cytokine release, and the incorporation of SIRPα knockdown to overcome the CD47
immune checkpoint. SIRPα knockdown is achieved using Carisma’s proprietary intronic
shRNA platform, which enables CAR delivery and gene knockdown using a single vector. The
Company is targeting an Investigational New Drug Application (IND) for CT-1119 in 2025. |
| · | In
Vivo CAR-M (Moderna Collaboration) |
| o | Presented
pre-clinical proof of concept data demonstrating feasibility, tolerability, and early efficacy
of mRNA/LNP in vivo CAR-M therapy at the Society for Immunotherapy of Cancer (SITC)
38th Annual Meeting. Accepted as a late-breaking abstract and oral presentation, “In
vivo CAR-M: Redirecting endogenous myeloid cells with mRNA for cancer immunotherapy,”
showcased data that demonstrated CAR-M can be directly produced in vivo, or within
the body, successfully redirecting endogenous myeloid cells against tumor-associated antigens
using mRNA/LNP. This novel approach to cancer immunotherapy offers an off-the-shelf solution
that has the potential to increase access to CAR-based therapies and be the basis of up to
12 oncology programs developed under the Carisma and Moderna collaboration. |
Upcoming
Milestones
| · | The
Company recently submitted an IND to the U.S. Food and Drug Administration (FDA) for CT-0525.
Subject to regulatory feedback, the Company expects to treat the first patient in the first
half of 2024. |
| · | The
Company expects to present data from the sub-study of its Phase 1 clinical trial of CT-0508
in combination with pembrolizumab in the first half of 2024. |
| · | The
Company expects pre-clinical proof of concept data for its initial program outside of oncology,
in liver fibrosis, in the first half of 2024. |
| · | The
Company is targeting an IND for CT-1119 in 2025. |
Third
Quarter 2023 Financial Results
| · | Cash,
cash equivalents and marketable securities as of September 30, 2023, were $94.1 million,
compared to $117.1 million as of June 30, 2023. |
| · | Research
& development expenses were $19.6 million for the third quarter of 2023, compared to
$15.6 million for the same period in 2022. The increase of $4.0 million was primarily due
to a $2.9 million increase in direct costs associated with the pre-clinical development of
CT-0525, a $1.2 million increase in personnel costs due to growth in research and development
employee headcount, and a $0.3 million increase in direct costs associated with the
pre-clinical development related to CT-1119, partially offset by a $0.2 million decrease
in direct costs associated with CT-0508 and a $0.1 million decrease of other clinical
and pre-clinical development expenses associated with tracking CT-0525 and CT-1119 separately. |
| · | General
& administrative expenses were $6.6 million for the third quarter of 2023, compared to
$3.8 million for the same period in 2022. The increase of $2.8 million was primarily due
to a $1.4 million increase of higher personnel costs as a result of an increase in headcount,
a $0.4 million increase in facilities and supplies due to an increase in office expenditures,
a $0.6 million increase in legal and professional fees in support of our patent portfolio
and expanding infrastructure, as well as a $0.4 million increase in other expenses due
to an increase in travel expenses and subscriptions. |
| · | Net
loss was $21.4 million for the third quarter of 2023, compared to net loss of $18.3 million
for the same period in 2022, primarily due to increased research and development expenses
to support CT-0525 as well as an increase in expanding headcount and infrastructure, which
was partially offset by Moderna collaboration revenue. |
Outlook
Carisma
believes that its cash, cash equivalents and marketable securities of $94.1 million as of September 30, 2023, are sufficient to sustain
Carisma's planned operations into the first quarter of 2025.
About
CT-0508
CT-0508
is a human epidermal growth factor receptor 2 (HER2) targeted chimeric antigen receptor macrophage (CAR-M). It is being evaluated in
a landmark Phase 1 multi-center clinical trial that focuses on patients with recurrent or metastatic HER2-overexpressing solid tumors
whose cancers do not have approved HER2-targeted therapies or who do not respond to treatment. Carisma is selecting participants who
have tumors of any anatomical origin, but with the commonality of overexpressing the HER2 receptor on the cell surface, which is the
target for its CAR-M. The Phase 1 clinical trial marks the first time that engineered macrophages are being studied in humans. The trial
continues to enroll patients at seven clinical sites in the U.S., including (i) the University of Pennsylvania Abramson Cancer Center,
(ii) the University of North Carolina Lineberger Comprehensive Cancer Center, (iii) the City of Hope National Medical Center, (iv) the
MD Anderson Cancer Center, (v) the Sarah Cannon Cancer Research Institute, (vi) Oregon Health & Science University and (vii) Fred
Hutchinson Cancer Center.
About
Carisma
Carisma
Therapeutics Inc. is a clinical stage biopharmaceutical company focused on utilizing our proprietary macrophage and monocyte cell engineering
platform to develop transformative immunotherapies to treat cancer and other serious diseases. We have created a comprehensive, differentiated
proprietary cell therapy platform focused on engineered macrophages and monocytes, cells that play a crucial role in both the innate
and adaptive immune response. Carisma is headquartered in Philadelphia, PA. For more information, please visit www.carismatx.com.
Cautionary
Note on Forward-Looking Statements
Statements
in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not
historical facts, may constitute “forward-looking statements” within the meaning of The Private Securities Litigation Reform
Act of 1995. These statements include, but are not limited to, statements relating to Carisma’s business, strategy, future operations,
cash runway, the advancement of Carisma’s product candidates and product pipeline, and clinical development of Carisma’s
product candidates, including expectations regarding timing of initiation and results of clinical trials. The words “anticipate,”
“believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,”
“goals,” “intend,” “may,” “might,” “outlook,” “plan,” “project,”
“potential,” “predict,” “target,” “possible,” “will,” “would,”
“could,” “should,” and similar expressions are intended to identify forward-looking statements, although not
all forward-looking statements contain these identifying words.
Any
forward-looking statements are based on management’s current expectations of future events and are subject to a number of risks
and uncertainties that could cause actual results to differ materially and adversely from those set forth in, or implied by, such forward-looking
statements. These risks and uncertainties include, but are not limited to, (i) Carisma’s ability to obtain, maintain and protect
its intellectual property rights related to its product candidates; (ii) Carisma’s ability to advance the development of its product
candidates under the timelines it anticipates in planned and future clinical trials; (iii) Carisma’s ability to replicate in later
clinical trials positive results found in preclinical studies and early-stage clinical trials of its product candidates; (iv) Carisma’s
ability to realize the anticipated benefits of its research and development programs, strategic partnerships, research and licensing
programs and academic and other collaborations; (v) regulatory requirements or developments and Carisma’s ability to obtain and
maintain necessary approvals from the U.S. Food and Drug Administration and other regulatory authorities related to its product candidates;
(vi) changes to clinical trial designs and regulatory pathways; (vii) risks associated with Carisma’s ability to manage expenses;
(viii) changes in capital resource requirements; (ix) risks related to the inability of Carisma to obtain sufficient additional capital
to continue to advance its product candidates and its preclinical programs; and (x) legislative, regulatory, political and economic developments.
For
a discussion of these risks and uncertainties, and other important factors, any of which could cause Carisma’s actual results to
differ from those contained in the forward-looking statements, see the “Risk Factors” set forth in the Company’s Quarterly
Report on Form 10-Q filed with the Securities and Exchange Commission on November 9, 2023, as well as discussions of potential risks,
uncertainties, and other important factors in Carisma’s other recent filings with the Securities and Exchange Commission. Any forward-looking
statements that are made in this press release speak as of the date of this press release. Carisma undertakes no obligation to revise
the forward-looking statements or to update them to reflect events or circumstances occurring after the date of this press release, whether
as a result of new information, future developments or otherwise, except as required by the federal securities laws.
Media
Contact:
Julia
Stern
(763)
350-5223
jstern@realchemistry.com
Investor
Contact:
investors@carismatx.com
CARISMA
THERAPEUTICS INC.
Unaudited
Consolidated Balance Sheets
(in
thousands, except share and per share data)
| |
September
30,
2023 | | |
December
31,
2022 | |
Assets | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash
and cash equivalents | |
$ | 83,132 | | |
$ | 24,194 | |
Marketable
securities | |
| 11,005 | | |
| 27,802 | |
Prepaid
expenses and other assets | |
| 3,428 | | |
| 2,596 | |
Total
current assets | |
| 97,565 | | |
| 54,592 | |
Property and equipment, net | |
| 7,379 | | |
| 8,628 | |
Right of use assets –
operating leases | |
| 1,664 | | |
| 4,822 | |
Restricted cash | |
| 30 | | |
| — | |
Deferred
financing costs | |
| 146 | | |
| 4,111 | |
Total
assets | |
$ | 106,784 | | |
$ | 72,153 | |
| |
| | | |
| | |
Liabilities, Convertible
Preferred Stock and Stockholders' Equity (Deficit) | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts
payable | |
$ | 2,409 | | |
$ | 1,728 | |
Accrued
expenses | |
| 7,026 | | |
| 10,361 | |
Deferred
revenue | |
| 1,185 | | |
| 2,459 | |
Operating
lease liabilities | |
| 856 | | |
| 3,437 | |
Finance
lease liabilities | |
| 532 | | |
| 1,162 | |
Other
current liabilities | |
| 943 | | |
| 523 | |
Total
current liabilities | |
| 12,951 | | |
| 19,670 | |
Deferred revenue | |
| 45,000 | | |
| 45,000 | |
Convertible promissory note | |
| — | | |
| 33,717 | |
Derivative liability | |
| — | | |
| 5,739 | |
Operating lease liabilities | |
| 891 | | |
| 976 | |
Finance lease liabilities | |
| 468 | | |
| 872 | |
Other long-term
liabilities | |
| 1,176 | | |
| 1,041 | |
Total
liabilities | |
| 60,486 | | |
| 107,015 | |
| |
| | | |
| | |
Convertible
preferred stock | |
| — | | |
| 107,808 | |
Stockholders’ equity (deficit): | |
| | | |
| | |
Common
stock $0.001 par value, 350,000,000 shares authorized, 40,304,436 and 2,217,737 shares issued and outstanding at September 30,
2023 and December 31, 2022, respectively | |
| 40 | | |
| 2 | |
Additional
paid-in capital | |
| 270,029 | | |
| 1,197 | |
Accumulated
other comprehensive income (loss) | |
| 373 | | |
| (41 | ) |
Accumulated
deficit | |
| (224,144 | ) | |
| (158,223 | ) |
Total
Carisma Therapeutics Inc. stockholders’ equity (deficit) | |
| 46,298 | | |
| (157,065 | ) |
Noncontrolling
interests | |
| — | | |
| 14,395 | |
Total
stockholders’ equity (deficit) | |
| 46,298 | | |
| (142,670 | ) |
Total
liabilities, convertible preferred stock and stockholders’ equity (deficit) | |
$ | 106,784 | | |
$ | 72,153 | |
CARISMA
THERAPEUTICS INC.
Unaudited
Consolidated Statements of Operations and Comprehensive Loss
(in
thousands, except share and per share data)
| |
Three
Months Ended September 30, | |
| |
2023 | | |
2022 | |
Collaboration
revenues | |
$ | 3,827 | | |
$ | 2,578 | |
Operating expenses: | |
| | | |
| | |
Research
and development | |
| 19,551 | | |
| 15,557 | |
General
and administrative | |
| 6,620 | | |
| 3,772 | |
Total
operating expenses | |
| 26,171 | | |
| 19,329 | |
Operating
loss | |
| (22,344 | ) | |
| (16,751 | ) |
Change in fair value of derivative
liability | |
| — | | |
| (668 | ) |
Interest
income (expense), net | |
| 941 | | |
| (908 | ) |
Pre-tax loss | |
| (21,403 | ) | |
| (18,327 | ) |
Income
tax expense | |
| — | | |
| — | |
Net loss | |
$ | (21,403 | ) | |
$ | (18,327 | ) |
| |
| | | |
| | |
Share information: | |
| | | |
| | |
Net loss
per share of common stock, basic and diluted | |
$ | (0.53 | ) | |
$ | (8.37 | ) |
Weighted-average
shares of common stock outstanding, basic and diluted | |
| 40,285,858 | | |
| 2,189,265 | |
Comprehensive loss | |
| | | |
| | |
Net loss | |
$ | (21,403 | ) | |
$ | (18,327 | ) |
Unrealized
gain (loss) on marketable securities | |
| 108 | | |
| 37 | |
Comprehensive
loss | |
$ | (21,295 | ) | |
$ | (18,290 | ) |
v3.23.3
X |
- DefinitionBoolean flag that is true when the XBRL content amends previously-filed or accepted submission.
+ References
+ Details
Name: |
dei_AmendmentFlag |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:booleanItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionFor 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
+ Details
Name: |
dei_DocumentPeriodEndDate |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:dateItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionThe 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
+ Details
Name: |
dei_DocumentType |
Namespace Prefix: |
dei_ |
Data Type: |
dei:submissionTypeItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionAddress Line 1 such as Attn, Building Name, Street Name
+ References
+ Details
Name: |
dei_EntityAddressAddressLine1 |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:normalizedStringItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionAddress Line 2 such as Street or Suite number
+ References
+ Details
Name: |
dei_EntityAddressAddressLine2 |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:normalizedStringItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- Definition
+ References
+ Details
Name: |
dei_EntityAddressCityOrTown |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:normalizedStringItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionCode for the postal or zip code
+ References
+ Details
Name: |
dei_EntityAddressPostalZipCode |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:normalizedStringItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionName of the state or province.
+ References
+ Details
Name: |
dei_EntityAddressStateOrProvince |
Namespace Prefix: |
dei_ |
Data Type: |
dei:stateOrProvinceItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionA unique 10-digit SEC-issued value to identify entities that have filed disclosures with the SEC. It is commonly abbreviated as CIK.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionIndicate if registrant meets the emerging growth company criteria.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionCommission 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
+ Details
Name: |
dei_EntityFileNumber |
Namespace Prefix: |
dei_ |
Data Type: |
dei:fileNumberItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionTwo-character EDGAR code representing the state or country of incorporation.
+ References
+ Details
Name: |
dei_EntityIncorporationStateCountryCode |
Namespace Prefix: |
dei_ |
Data Type: |
dei:edgarStateCountryItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionThe exact name of the entity filing the report as specified in its charter, which is required by forms filed with the SEC.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionThe Tax Identification Number (TIN), also known as an Employer Identification Number (EIN), is a unique 9-digit value assigned by the IRS.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionLocal phone number for entity.
+ References
+ Details
Name: |
dei_LocalPhoneNumber |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:normalizedStringItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionBoolean 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.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionBoolean 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.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionTitle of a 12(b) registered security.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionName of the Exchange on which a security is registered.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
X |
- DefinitionBoolean 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.
+ ReferencesReference 1: http://www.xbrl.org/2003/role/presentationRef -Publisher SEC -Name Exchange Act -Section 14a -Number 240 -Subsection 12
+ Details
Name: |
dei_SolicitingMaterial |
Namespace Prefix: |
dei_ |
Data Type: |
xbrli:booleanItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionTrading symbol of an instrument as listed on an exchange.
+ References
+ Details
Name: |
dei_TradingSymbol |
Namespace Prefix: |
dei_ |
Data Type: |
dei:tradingSymbolItemType |
Balance Type: |
na |
Period Type: |
duration |
|
X |
- DefinitionBoolean 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.
+ ReferencesReference 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: |
na |
Period Type: |
duration |
|
Carisma Therapeutics (NASDAQ:CARM)
과거 데이터 주식 차트
부터 5월(5) 2024 으로 6월(6) 2024
Carisma Therapeutics (NASDAQ:CARM)
과거 데이터 주식 차트
부터 6월(6) 2023 으로 6월(6) 2024