Please wait while we load the requested 10-Q report or click the link below:
https://last10k.com/sec-filings/report/1435049/000156459022019844/kdny-10q_20220331.htm
August 2023
August 2023
July 2023
June 2023
June 2023
June 2023
June 2023
May 2023
April 2023
March 2023
Exhibit 99.1
Chinook Therapeutics Provides Business Update and Reports First Quarter 2022 Financial Results
SEATTLE May 12, 2022 – Chinook Therapeutics, Inc. (Nasdaq: KDNY), a biopharmaceutical company focused on the discovery, development and commercialization of precision medicines for kidney diseases, today provided a business update and reported financial results for the first quarter ended March 31, 2022.
“During the first quarter of 2022, we made strong progress advancing our pipeline of clinical, research and discovery programs for rare, severe chronic kidney diseases. We continue to enroll patients in the phase 3 ALIGN and phase 2 AFFINITY trials for atrasentan as well as the phase 1/2 trial of BION-1301, and we are pleased to have recently initiated the phase 1 healthy volunteer trial of CHK-336, our first internally-discovered program for the treatment of primary and idiopathic hyperoxaluria,” said Eric Dobmeier, president and chief executive officer of Chinook Therapeutics. “We look forward to the upcoming 59th ERA Congress being held May 19th – 22nd, where we will present clinical data from both our lead programs, atrasentan and BION-1301, in patients with IgA nephropathy (IgAN).”
Recent Accomplishments and Updates
Atrasentan
Atrasentan is a potent and selective endothelin A (ETA) receptor antagonist that has the potential to provide benefit in multiple chronic kidney diseases by reducing proteinuria and having direct anti-inflammatory and anti-fibrotic effects to preserve kidney function. The phase 3 ALIGN trial of atrasentan is currently enrolling patients with IgAN, and the phase 2 AFFINITY basket trial of atrasentan is currently enrolling patients with proteinuric glomerular diseases.
|
• |
Enrollment of the phase 3 ALIGN trial of atrasentan continues to advance with the activation of new trial sites and expansion into additional countries. Chinook expects to report topline data from the six-month interim proteinuria endpoint analysis in 2023 to support an application for accelerated approval under Subpart H in the United States. |
|
• |
Chinook plans to present data from the IgAN patient cohort of the phase 2 AFFINITY trial in an oral presentation at the 59th ERA Congress on May 20, 2022, and provide a program update on atrasentan during an investor conference call and webcast at 4:15 pm EDT that day. Chinook has completed enrollment of the IgAN patient cohort of this trial, and continues to enroll the other three cohorts, including patients with focal segmental glomerulosclerosis (FSGS), Alport syndrome and diabetic kidney disease in combination with SGLT2 inhibitors. |
|
• |
Chinook will deliver a mini-oral presentation at the 59th ERA Congress on May 19, 2022 on preclinical mechanistic work describing atrasentan’s effect to block mesangial cell injury and the pathogenic transcriptional networks driving IgAN progression in a model system. |
|
• |
In March 2022, Chinook presented an overview of the phase 2 AFFINITY clinical trial at the 4th Annual Chronic Kidney Disease (CKD) Drug Development Summit. |
|
• |
In February 2022, Chinook delivered an encore trials-in-progress presentations on the phase 3 ALIGN and phase 2 AFFINITY clinical trials at the ISN World Congress of Nephrology 2022. |
Please wait while we load the requested 10-Q report or click the link below:
https://last10k.com/sec-filings/report/1435049/000156459022019844/kdny-10q_20220331.htm
Compare this 10-Q Quarterly Report to its predecessor by reading our highlights to see what text and tables were removed , added and changed by Aduro Biotech, Inc..
Aduro Biotech, Inc.'s Definitive Proxy Statement (Form DEF 14A) filed after their 2022 10-K Annual Report includes:
Rating
Learn More
The decrease in general and administrative expenses was primarily due to lower consulting and other professional services costs; lower employee-related costs, including salaries and benefits; and a decrease in facilities and other costs.
Change in fair value of contingent consideration and contingent value rights liabilities Change in fair value of contingent consideration and contingent value rights liabilities was a benefit of $1.0 million for the three months ended March 31, 2022, a decrease of $2.9 million compared to expense of $1.8 million the three months ended March 31, 2021.
Research and development costs include employee-related costs; licensing costs; materials and supplies; contracted research and manufacturing; consulting arrangements; allocated costs, such as facility costs; and other expenses incurred to advance our research and development activities.
At the same time, we expect our expenses to increase in connection with our ongoing development activities, particularly as we continue the research, development and clinical trials of, and seek regulatory approval for, our product candidates.
The increase in cash used was primarily due to purchases of marketable securities, net of proceeds from maturities of marketable securities.
Amortization of intangible assets Amortization...Read more
In April 2021, we entered...Read more
We expect that our research...Read more
The following table summarizes our...Read more
The increase was due to...Read more
Investing Activities Net cash used...Read more
Financing Activities Net cash provided...Read more
We will pay the sales...Read more
We expect our research and...Read more
Share of net loss of...Read more
At the effective time of...Read more
Amortization of intangible assets, excluding...Read more
If we raise additional funds...Read more
Collaboration and License Revenue Total...Read more
As of March 31, 2022,...Read more
Potential milestone payments related to...Read more
The terms of such agreements...Read more
General and Administrative Expenses The...Read more
Share of net loss of...Read more
The decrease resulted from an...Read more
However, due to a low...Read more
We believe that a strong...Read more
Employee-related costs consist of salaries,...Read more
As a result of the...Read more
A holder of Pre-Funded Warrants...Read more
Research and development expenses represent...Read more
The application of systems biology...Read more
The pharmacokinetics of BION-1301 observed...Read more
Financial Statements, Disclosures and Schedules
Inside this 10-Q Quarterly Report
Material Contracts, Statements, Certifications & more
Aduro Biotech, Inc. provided additional information to their SEC Filing as exhibits
Ticker: KDNY
CIK: 1435049
Form Type: 10-Q Quarterly Report
Accession Number: 0001564590-22-019844
Submitted to the SEC: Thu May 12 2022 4:06:35 PM EST
Accepted by the SEC: Thu May 12 2022
Period: Thursday, March 31, 2022
Industry: Pharmaceutical Preparations