0001730430
false
0001730430
2023-10-31
2023-10-31
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):
October 31, 2023
Kiniksa Pharmaceuticals, Ltd.
(Exact name of Registrant as Specified in Its
Charter)
Bermuda |
|
001-730430 |
|
98-1327726 |
(State or other jurisdiction of
incorporation or organization) |
|
(Commission
File Number) |
|
(I.R.S. Employer
Identification No.) |
Kiniksa Pharmaceuticals, Ltd.
Clarendon House
2 Church Street
Hamilton HM11, Bermuda
(808) 451-3453
(Address, zip code and telephone number,
including area code of principal executive offices)
Kiniksa Pharmaceuticals Corp.
100 Hayden Avenue
Lexington, MA, 02421
(781) 431-9100
(Address, zip code and telephone number,
including area code of agent for service)
N/A
(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
| ¨ | 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 each exchange on which
registered |
Class A
Common Shares $0.000273235 par value |
|
KNSA |
|
The Nasdaq Stock Market LLC |
|
|
|
|
(Nasdaq Global Select Market) |
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 October 31, 2023, Kiniksa Pharmaceuticals, Ltd.
issued a press release announcing financial results for the quarter ended September 30, 2023. A copy of the press release is furnished
with this Current Report on Form 8-K as Exhibit 99.1.
The information contained in this Item 2.02 of this
Current Report on Form 8-K and Exhibit 99.1 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 under the Securities Act of 1933, as amended, or the Exchange Act, regardless of
any general incorporation language in such filing and except as expressly provided by specific reference in such filing.
Item 9.01. Financial Statements and Exhibits.
(d) 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.
|
KINIKSA PHARMACEUTICALS, LTD. |
|
|
Date: October 31,
2023 |
By: |
/s/
Madelyn Zeylikman |
|
|
Madelyn Zeylikman |
|
|
Senior Vice President, General Counsel and Secretary |
Exhibit 99.1
Kiniksa Pharmaceuticals
Reports Third Quarter 2023 Financial Results and Recent Portfolio Execution
– ARCALYST®
(rilonacept) Q3 2023 net product revenue of $64.8 million, representing ~94% year-over-year growth –
– KPL-404
Phase 2 rheumatoid arthritis data from Cohorts 1-3 now expected in Q1 2024 –
– Cash
reserves of $201 million expected to fund operations into at least 2027 –
– Conference
call and webcast scheduled for 8:30 am ET today –
HAMILTON,
BERMUDA – October 31, 2023 – Kiniksa
Pharmaceuticals, Ltd. (Nasdaq: KNSA) (Kiniksa), a biopharmaceutical company with a pipeline of immune-modulating assets designed
to target a spectrum of cardiovascular and autoimmune diseases, today reported third quarter 2023 financial results and recent portfolio
execution.
“We continue to advance all aspects
of our business, including strong revenue growth with ARCALYST and clinical trial execution with KPL-404, and we have cash runway into
at least 2027,” said Sanj K. Patel, Chairman and Chief Executive Officer of Kiniksa. “On the commercial side, we are building
the recurrent pericarditis market and are focused on helping as many patients as possible. We are currently tracking to the high end
of our previously issued guidance of $220 million to $230 million in product revenue. Within our clinical development portfolio, we have
completed enrollment in the third cohort of the Phase 2 trial of KPL-404 in rheumatoid arthritis. We now expect data from Cohorts 1-3
in the first quarter of 2024.”
Portfolio Execution
ARCALYST (IL-1α and IL-1β
cytokine trap)
| · | ARCALYST
net product revenue was $64.8 million for the third quarter of 2023. |
| · | Since
launch, more than 1,450 prescribers have written ARCALYST prescriptions for recurrent pericarditis. |
| · | As
of the end of the third quarter of 2023, average total duration of ARCALYST therapy in recurrent
pericarditis was approximately 20 months. |
| - | Average
total duration of therapy includes the approximately 45% of patients who restarted ARCALYST,
within an average of 8 weeks, after having discontinued therapy. |
KPL-404 (monoclonal antibody inhibitor
of CD40-CD154 interaction)
| · | Kiniksa
completed enrollment of the third cohort of the Phase 2 clinical trial of KPL-404 in rheumatoid
arthritis. The company now expects data from Cohorts 1-3 in the first quarter of 2024. |
| · | Kiniksa
is currently enrolling a fourth cohort (Cohort 4) of the Phase 2 clinical trial of KPL-404
in rheumatoid arthritis. The additional cohort will evaluate a fixed dose level administered
as a single subcutaneous injection once monthly. The company expects data from Cohort 4 in
the second quarter of 2024. |
Mavrilimumab (monoclonal antibody
inhibitor targeting GM-CSFRα)
| · | Kiniksa
is pursuing collaborative study agreements to evaluate the potential of mavrilimumab in rare
cardiovascular diseases where the granulocyte macrophage colony stimulating factor (GM-CSF)
mechanism has been implicated. |
Financial Results
| · | ARCALYST
net product revenue for the third quarter of 2023 was $64.8 million, compared to $33.4 million
for the third quarter of 2022. |
| - | Total
revenue for the third quarter of 2023 was $67.0 million, including $2.2 million in license
and collaboration revenue, compared to total revenue for the third quarter of 2022 of $99.1
million, including $65.7 million in license and collaboration revenue. |
| · | Total
operating expenses for the third quarter of 2023 were $78.0 million, compared to $52.7 million
for the third quarter of 2022. |
| - | Total
operating expenses for the third quarter of 2023 included $17.3 million in collaboration
expenses, due to increasing ARCALYST profitability, compared to $4.6 million for the third
quarter of 2022. |
| - | Total
operating expenses for the third quarter of 2023 included $6.8 million in non-cash, share-based
compensation expense, compared to $6.0 million for the third quarter of 2022. |
| · | Net
loss for the third quarter of 2023 was $13.9 million, compared to net income of $224.1 million
for the third quarter of 2022. |
| · | As
of September 30, 2023, Kiniksa had $201.1 million of cash, cash equivalents, and short-term
investments and no debt. |
Financial
Guidance
| · | Kiniksa
expects 2023 ARCALYST net product revenue of between $220 million and $230 million. |
| · | Kiniksa
expects that its cash, cash equivalents, and short-term investments will fund its current
operating plan into at least 2027. |
Conference
Call Information
| · | Kiniksa
will host a conference call and webcast at 8:30 a.m. Eastern Time on Tuesday, October 31,
2023, to discuss third quarter 2023 financial results and recent portfolio execution. |
| · | Individuals
interested in participating in the call via telephone may register here. Upon registration,
all telephone participants will receive a confirmation email detailing how to join the conference
call, including the dial-in number along with a unique passcode and registrant ID that can
be used to access the call. To access the webcast, please visit the Investors and Media section
of Kiniksa’s website. A replay of the event will also be available on Kiniksa’s
website within approximately 48 hours after the event. |
About Kiniksa
Kiniksa is a biopharmaceutical company
focused on discovering, acquiring, developing, and commercializing therapeutic medicines for patients suffering from debilitating diseases
with significant unmet medical need. Kiniksa’s immune-modulating assets, ARCALYST, KPL-404, and mavrilimumab, are based on strong
biologic rationale or validated mechanisms, target a spectrum of underserved cardiovascular and autoimmune conditions, and offer the
potential for differentiation. For more information, please visit www.kiniksa.com.
About ARCALYST
ARCALYST is
a weekly, subcutaneously injected recombinant dimeric fusion protein that blocks interleukin-1 alpha (IL-1α) and interleukin-1
beta (IL-1β) signaling. ARCALYST was discovered by Regeneron Pharmaceuticals, Inc. (Regeneron) and is approved by the U.S.
Food and Drug Administration (FDA) for recurrent pericarditis, cryopyrin-associated periodic syndromes (CAPS), including Familial Cold
Autoinflammatory Syndrome and Muckle-Wells Syndrome, and deficiency of IL-1 receptor antagonist (DIRA). The FDA granted Breakthrough
Therapy designation to ARCALYST for the treatment of recurrent pericarditis in 2019 and Orphan Drug exclusivity
to ARCALYST in 2021 for the treatment of recurrent
pericarditis and reduction in risk of recurrence in adults and pediatric patients 12 years
and older. The European Commission granted Orphan Drug Designation to ARCALYST for the treatment
of idiopathic pericarditis in 2021.
IMPORTANT
SAFETY INFORMATION ABOUT ARCALYST
| · | ARCALYST
may affect your immune system and can lower the ability of your immune system to fight infections.
Serious infections, including life-threatening infections and death, have happened in patients
taking ARCALYST. If you have any signs of an infection, call your doctor right away. Treatment
with ARCALYST should be stopped if you get a serious infection. You should not begin treatment
with ARCALYST if you have an infection or have infections that keep coming back (chronic
infection). |
| · | While
taking ARCALYST, do not take other medicines that block interleukin-1, such as Kineret®
(anakinra), or medicines that block tumor necrosis factor, such as Enbrel®
(etanercept), Humira® (adalimumab), or Remicade® (infliximab),
as this may increase your risk of getting a serious infection. |
| · | Talk
with your doctor about your vaccine history. Ask your doctor whether you should receive any
vaccines before you begin treatment with ARCALYST. |
| · | Medicines
that affect the immune system may increase the risk of getting cancer. |
| · | Stop
taking ARCALYST and call your doctor or get emergency care right away if you have any symptoms
of an allergic reaction. |
| · | Your
doctor will do blood tests to check for changes in your blood cholesterol and triglycerides. |
| · | Common
side effects include injection-site reactions (which may include pain, redness, swelling,
itching, bruising, lumps, inflammation, skin rash, blisters, warmth, and bleeding at the
injection site), upper respiratory tract infections, joint and muscle aches, rash, ear infection,
sore throat, and runny nose. |
For
more information about ARCALYST, talk to your doctor and see the Product Information.
About KPL-404
KPL-404 is
an investigational humanized monoclonal antibody that is designed to inhibit CD40-CD154 (CD40 ligand) interaction, a key T-cell co-stimulatory
signal critical for B-cell maturation and immunoglobulin class switching and Type 1 immune responses. Kiniksa believes disrupting the
CD40-CD154 interaction is an attractive approach to address multiple autoimmune disease pathologies.
About Mavrilimumab
Mavrilimumab
is an investigational fully human monoclonal antibody that blocks activity of GM-CSF by specifically binding to the alpha subunit of
the GM-CSF receptor (GM-CSFRα). Phase 2 clinical trials of mavrilimumab in rheumatoid arthritis and giant cell arteritis achieved
their primary and secondary endpoints with statistical significance. Kiniksa is evaluating the development of mavrilimumab in rare cardiovascular
diseases where the GM-CSF mechanism has been implicated.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of the Private Securities Litigation Reform Act of 1995. In some cases, you can identify forward looking
statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,”
“could,” “intend,” “target,” “project,” “contemplate,” “believe,”
“estimate,” “predict,” “potential” or “continue” or the negative of these terms or other
similar expressions, although not all forward-looking statements contain these identifying words. All statements contained in this press
release that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation,
statements regarding: our expectation that we will report data from cohorts 1-3 of our Phase 2 clinical trial of KPL-404 in rheumatoid
arthritis in the first quarter of 2024 and data from cohort 4 of such trial in the second quarter of 2024; our expectation that our full-year
net product revenue will be at the high end of our $220 million to $230 million guidance range; our expectation about our cash reserves
funding our current operating plan into at least 2027; our beliefs about the mechanisms of action of our product candidates and potential
impact of their approach, including that using KPL-404 to disrupt the CD40-CD154 interaction is an attractive approach to address multiple
autoimmune disease pathologies; and our belief that all of our product candidates offer the potential for differentiation.
These forward-looking statements are
based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown
risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different
from any future results, performance or achievements expressed or implied by the forward-looking statements, including without limitation,
the following: delays or difficulty in enrollment of patients in, and activation or continuation of sites for, our clinical trials; delays
or difficulty in completing our clinical trials as originally designed; potential for changes between final data and any preliminary,
interim, top-line or other data from clinical trials; our inability to replicate results from our earlier clinical trials or studies;
impact of additional data from us or other companies, including the potential for our data to produce negative, inconclusive or commercially
uncompetitive results; potential undesirable side effects caused by our products and product candidates; our inability to demonstrate
safety and efficacy to the satisfaction of applicable regulatory authorities; potential for applicable regulatory authorities to not
accept our filings, delay or deny approval of any of our product candidates or require additional data or trials to support approval;
inability to successfully execute on our commercial strategy for ARCALYST; our reliance on third parties as the sole source of supply
of the drug substance and drug product used in our products and product candidates; our reliance on Regeneron as the current sole manufacturer
of ARCALYST; risks arising from our ongoing technology transfer of ARCALYST drug substance manufacturing; raw material, important ancillary
product and drug substance and/or drug product shortages; our reliance on third parties to conduct research, clinical trials, and/or
certain regulatory activities for our product candidates; complications in coordinating requirements, regulations and guidelines of regulatory
authorities across jurisdictions for our clinical trials; changes in our operating plan, business development strategy or funding requirements;
and existing or new competition.
These and other important factors discussed
in our filings with the U.S. Securities and Exchange Commission, including under the caption “Risk Factors” contained therein,
could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any
such forward-looking statements represent management’s estimates as of the date of this press release. Except as required by law,
we disclaim any intention or obligation to update or revise any forward-looking statements. These forward-looking statements should not
be relied upon as representing our views as of any date subsequent to the date of this press release.
ARCALYST® is a registered
trademark of Regeneron. All other trademarks are the property of their respective owners.
Every Second Counts!
®
Kiniksa Investor and Media Contact
Rachel Frank
(339) 970-9437
rfrank@kiniksa.com
KINIKSA
PHARMACEUTICALS, LTD.
SELECTED
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME (LOSS)
(In
thousands)
(Unaudited)
| |
Three Months Ended | | |
Nine Months Ended | |
| |
September 30, | | |
September 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Revenue: | |
| | | |
| | | |
| | | |
| | |
Product revenue, net | |
$ | 64,802 | | |
$ | 33,424 | | |
$ | 161,956 | | |
$ | 82,585 | |
License and collaboration
revenue | |
| 2,244 | | |
| 65,711 | | |
| 24,908 | | |
| 75,711 | |
Total revenue | |
| 67,046 | | |
| 99,135 | | |
| 186,864 | | |
| 158,296 | |
Costs and operating expenses: | |
| | | |
| | | |
| | | |
| | |
Cost of goods sold | |
| 9,088 | | |
| 6,937 | | |
| 23,823 | | |
| 16,185 | |
Collaboration expenses | |
| 17,311 | | |
| 4,623 | | |
| 39,585 | | |
| 16,549 | |
Research and development | |
| 17,106 | | |
| 16,485 | | |
| 56,045 | | |
| 51,100 | |
Selling, general
and administrative | |
| 34,468 | | |
| 24,677 | | |
| 92,688 | | |
| 70,736 | |
Total operating
expenses | |
| 77,973 | | |
| 52,722 | | |
| 212,141 | | |
| 154,570 | |
Income (loss) from operations | |
| (10,927 | ) | |
| 46,413 | | |
| (25,277 | ) | |
| 3,726 | |
Other income | |
| 2,428 | | |
| 322 | | |
| 6,175 | | |
| 459 | |
Income (loss) before income taxes | |
| (8,499 | ) | |
| 46,735 | | |
| (19,102 | ) | |
| 4,185 | |
Benefit (provision) for income taxes | |
| (5,356 | ) | |
| 177,358 | | |
| 7,949 | | |
| 174,717 | |
Net income (loss) | |
$ | (13,855 | ) | |
$ | 224,093 | | |
$ | (11,153 | ) | |
$ | 178,902 | |
Net income (loss) per share attributable to common shareholders—basic | |
$ | (0.20 | ) | |
$ | 3.23 | | |
$ | (0.16 | ) | |
$ | 2.58 | |
Net income (loss) per share attributable
to common shareholders—diluted | |
$ | (0.20 | ) | |
$ | 3.18 | | |
$ | (0.16 | ) | |
$ | 2.55 | |
Weighted average common shares outstanding—basic | |
| 70,186,016 | | |
| 69,445,071 | | |
| 69,953,591 | | |
| 69,305,755 | |
Weighted average common shares outstanding—diluted | |
| 70,186,016 | | |
| 70,552,018 | | |
| 69,953,591 | | |
| 70,286,444 | |
KINIKSA
PHARMACEUTICALS, LTD.
SELECTED
CONSOLIDATED BALANCE SHEET DATA
(In
thousands)
(Unaudited)
| |
As of | |
| |
September 30, | | |
December 31, | |
| |
2023 | | |
2022 | |
Cash, cash equivalents, and short-term investments | |
$ | 201,084 | | |
$ | 190,608 | |
Working capital | |
| 202,641 | | |
| 195,994 | |
Total assets | |
| 483,063 | | |
| 459,672 | |
Accumulated deficit | |
| (503,187 | ) | |
| (492,034 | ) |
Total shareholders' equity | |
| 405,127 | | |
| 396,149 | |
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 |
- DefinitionISO 3166-1 alpha-2 country code.
+ References
+ Details
Name: |
dei_EntityAddressCountry |
Namespace Prefix: |
dei_ |
Data Type: |
dei:countryCodeItemType |
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 |
- 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 |
|
Kiniksa Pharmaceuticals (NASDAQ:KNSA)
Historical Stock Chart
Von Apr 2024 bis Mai 2024
Kiniksa Pharmaceuticals (NASDAQ:KNSA)
Historical Stock Chart
Von Mai 2023 bis Mai 2024