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Cover Page - USD ($) | 12 Months Ended | |
---|---|---|
Dec. 31, 2020 | Mar. 29, 2021 | |
Document Information [Line Items] | ||
Document Type | 10-K | |
Amendment Flag | false | |
Document Period End Date | Dec. 31, 2020 | |
Document Fiscal Year Focus | 2020 | |
Document Fiscal Period Focus | FY | |
Document Annual Report | true | |
Document Transition Report | false | |
Entity Interactive Data Current | Yes | |
Entity Registrant Name | Checkmate Pharmaceuticals, Inc. | |
Entity Central Index Key | 0001651431 | |
Current Fiscal Year End Date | --12-31 | |
Entity Current Reporting Status | Yes | |
Entity Well-known Seasoned Issuer | No | |
Entity Voluntary Filers | No | |
Entity Shell Company | false | |
Entity Filer Category | Non-accelerated Filer | |
Entity Small Business | true | |
Entity Emerging Growth Company | true | |
Entity Ex Transition Period | false | |
Entity Incorporation, State or Country Code | DE | |
Entity Address, State or Province | DE | |
Entity Address, Country | MA | |
Title of 12(b) Security | Common Stock | |
Trading Symbol | CMPI | |
Security Exchange Name | NASDAQ | |
Entity Public Float | $ 314,566,207 | |
Entity Common Stock, Shares Outstanding | 21,618,395 | |
ICFR Auditor Attestation Flag | false |
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Compare this 10-K Annual Report to its predecessor by reading our highlights to see what text and tables were removed , added and changed by Checkmate Pharmaceuticals, Inc..
Checkmate Pharmaceuticals, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2021 10-K Annual Report includes:
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These payments are comprised of a license fee of $1.0 million which was recognized in research and development expense in 2015, a $1.0 million milestone payment in connection with the dosing of the first patient in our first Phase 1 clinical trial, which was recognized in research and development expense in 2016, and a $0.3 million license amendment fee in connection with the signing of the second amendment to the Kuros License Agreement, which was recognized in research and development expense in 2018.
We also anticipate that we will experience a significant increase in accounting, audit, legal, regulatory, compliance and director and officer insurance costs as well as investor and public relations expenses associated with operating as a public company.
We expect to continue to incur significant expenses and to increase operating losses for at least the next several years.
We have incurred recurring losses and had negative operating cash flows since inception and our ability to generate product revenue sufficient to achieve profitability will depend heavily on the successful development and eventual commercialization of CMP-001 or any other products we acquire or develop.
We expect our expenses to increase substantially in connection with our ongoing activities, particularly as we advance the preclinical activities and clinical trials for CMP-001 and any other product candidates that we may develop or acquire in the future.
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Financial Statements, Disclosures and Schedules
Inside this 10-K Annual Report
Material Contracts, Statements, Certifications & more
Checkmate Pharmaceuticals, Inc. provided additional information to their SEC Filing as exhibits
Ticker: CMPI
CIK: 1651431
Form Type: 10-K Annual Report
Accession Number: 0001193125-21-098414
Submitted to the SEC: Mon Mar 29 2021 4:52:25 PM EST
Accepted by the SEC: Mon Mar 29 2021
Period: Thursday, December 31, 2020
Industry: Biological Products No Disgnostic Substances