Deciphera Presents Data from QINLOCK® (Ripretinib) Program at the Connective Tissue Oncology Society (CTOS) 2020 Virtual Annual Meeting

On November 11, 2020 Deciphera Pharmaceuticals, Inc. (NASDAQ:DCPH), reported data presentations from clinical studies of QINLOCK, the Company’s switch-control tyrosine kinase inhibitor approved in the U.S. for fourth-line gastrointestinal stromal tumor (GIST), to be presented at the CTOS 2020 Virtual Annual Meeting, being held November 18-21, 2020 (Press release, Deciphera Pharmaceuticals, NOV 11, 2020, View Source [SID1234570584]). Posters and presentations are available to meeting participants as of November 11, 2020. New data presented at the meeting included an oral presentation titled "Characterization of the extensive heterogeneity of KIT/PDGFRA mutations in patients with fourth-line advanced gastrointestinal stromal tumor: Genomic analysis of the phase 3 INVICTUS study" and a poster presentation titled "Ripretinib demonstrated activity across all KIT/PDGFRA mutations in patients with fourth-line advanced gastrointestinal stromal tumor: Analysis from the phase 3 INVICTUS study".

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"We’re pleased to share our findings from the largest dataset of tumor and plasma sequencing in the fourth-line and fourth-line plus setting in GIST, which highlight the broad spectrum of mutations that drive this disease," said Matthew L. Sherman, MD, Executive Vice President and Chief Medical Officer of Deciphera. "Data being presented at CTOS also provide further evidence that QINLOCK inhibits a broad spectrum of relevant mutations in patients with advanced GIST who have received prior treatment with 3 or more kinase inhibitors, including imatinib."

Characterization of the extensive heterogeneity of KIT/PDGFRA mutations in patients with fourth-line advanced gastrointestinal stromal tumor: Genomic analysis of the phase 3 INVICTUS study

The INVICTUS Phase 3 clinical study is a randomized (2:1), double-blind, placebo-controlled, international, multicenter study to evaluate the safety, tolerability, and efficacy of QINLOCK compared to placebo in patients with advanced GIST whose previous therapies have included at least imatinib, sunitinib, and regorafenib. Baseline tumor and plasma samples were collected to investigate the genomic heterogeneity of resistance in the INVICTUS study.

This is the first and largest baseline genomic analysis by tumor and liquid biopsy in fourth-line patients with GIST that failed prior treatment with at least imatinib, sunitinib, and regorafenib.
In patients with fourth-line and fourth-line plus GIST, data demonstrated a complex and heterogenous mutational landscape.
The most frequent primary mutations found were in KIT exon 11 and KIT exon 9.
By tumor biopsy, secondary mutations were more diverse in KIT exons 17/18 (15 unique mutations) compared to KIT exons 13/14 (5 unique mutations).
More mutations were detected by liquid biopsy compared with tumor biopsy, increasing the detection rate of secondary mutations from 15 to 26 unique mutations (73% increase) in KIT exons 17/18 and from 5 to 12 unique mutations (140% increase) in KIT exons 13/14.
The heterogeneity of the KIT mutations highlight the need for therapies that are effective against a broad spectrum of mutations.
Ripretinib demonstrated activity across all KIT/PDGFRA mutations in patients with fourth-line advanced gastrointestinal stromal tumor: Analysis from the phase 3 INVICTUS study

Results from an exploratory analysis from the Phase 3 INVICTUS study showed that QINLOCK demonstrated clinically meaningful activity in patients with a broad spectrum of KIT and PDGFRA mutations. The data cutoff for this analysis was March 9, 2020.

In INVICTUS, QINLOCK demonstrated clinically meaningful activity in patients with fourth-line and fourth-line plus GIST (n=129) with multiple, heterogeneous genetic subsets of KIT/PDGFRA mutations. QINLOCK showed a median progression free survival (PFS) benefit of 6.3 months versus placebo of 1 month in all patients (hazard ratio = 0.16). Hazard ratios (HRs) of PFS by KIT mutation subgroup by combined tumor and liquid biopsy are below:

Mutation subgroup

QINLOCK 150 mg QD (N)

Placebo (N)

Hazard ratio (95% CI)

Any KIT exon 11a

52

34

0.13 (0.07, 0.24)

Any KIT exon 9a

16

7

0.22 (0.08, 0.63)

Any KIT exon 13

27

16

0.17 (0.08, 0.38)

Any KIT exon 17

44

27

0.14 (0.07, 0.28)

aOne patient had both KIT exon 11 and KIT exon 9 mutations detected in liquid biopsy. N, number of patients.

The HRs of PFS within different mutation subgroups all favored treatment with QINLOCK, which is in line with the primary outcome of the INVICTUS study. These results support the proposed broad mechanism of action of QINLOCK with its specific receptor binding properties.

The Company also announced two encore presentations highlighting data from the QINLOCK program, one oral presentation and one poster presentation, which will be featured at the CTOS 2020 Virtual Annual Meeting. The oral presentation will focus on results from the ongoing Phase 1 study of QINLOCK in patients with second-line through fourth-line plus GIST. The results demonstrate that patients receiving QINLOCK who, upon disease progression, dose escalated to QINLOCK 150 mg twice daily experienced additional, clinically meaningful, PFS benefit across all lines of therapy. The poster presentation will feature the nine-month follow-up data from the Phase 3 INVICTUS study in patients with fourth-line and fourth-line plus GIST.

About QINLOCK (ripretinib)

QINLOCK is a switch-control tyrosine kinase inhibitor that was engineered to broadly inhibit KIT and PDGFRA mutated kinases by using a dual mechanism of action that regulates the kinase switch pocket and activation loop. QINLOCK inhibits primary and secondary KIT mutations in exons 9, 11, 13, 14, 17, and 18 involved in GIST, as well as the primary exon 17 D816V mutation. QINLOCK also inhibits primary PDGFRA mutations in exons 12, 14, and 18, including the exon 18 D842V mutation, involved in a subset of GIST.

QINLOCK is approved by the U.S. FDA for the treatment of adult patients with advanced GIST who have received prior treatment with three or more kinase inhibitors, including imatinib. It is also approved by Health Canada for the treatment of adult patients with advanced GIST who have received prior treatment with imatinib, sunitinib, and regorafenib and by the Australian Therapeutic Goods Administration for the treatment of adult patients with advanced GIST who have received prior treatment with three or more kinase inhibitors, including imatinib.

U.S. Indication and Important Safety Information About QINLOCK

Indications and Usage

QINLOCK (ripretinib) is a kinase inhibitor indicated for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib. For more information visit QINLOCK.com.

Important Safety Information

There are no contraindications for QINLOCK.

Palmar-plantar erythrodysesthesia syndrome (PPES): In INVICTUS, Grade 1-2 PPES occurred in 21% of the 85 patients who received QINLOCK. PPES led to dose discontinuation in 1.2% of patients, dose interruption in 2.4% of patients, and dose reduction in 1.2% of patients. Based on severity, withhold QINLOCK and then resume at same or reduced dose.

New Primary Cutaneous Malignancies: In INVICTUS, cutaneous squamous cell carcinoma (cuSCC) occurred in 4.7% of the 85 patients who received QINLOCK with a median time to event of 4.6 months (range 3.8 to 6 months). In the pooled safety population, cuSCC and keratoacanthoma occurred in 7% and 1.9% of 351 patients, respectively. In INVICTUS, melanoma occurred in 2.4% of the 85 patients who received QINLOCK. In the pooled safety population, melanoma occurred in 0.9% of 351 patients. Perform dermatologic evaluations when initiating QINLOCK and routinely during treatment. Manage suspicious skin lesions with excision and dermatopathologic evaluation. Continue QINLOCK at the same dose.

Hypertension: In INVICTUS, Grade 1-3 hypertension occurred in 14% of the 85 patients who received QINLOCK, including Grade 3 hypertension in 7% of patients. Do not initiate QINLOCK in patients with uncontrolled hypertension. Monitor blood pressure as clinically indicated. Based on severity, withhold QINLOCK and then resume at same or reduced dose or permanently discontinue.

Cardiac Dysfunction: In INVICTUS, cardiac failure occurred in 1.2% of the 85 patients who received QINLOCK. In the pooled safety population, cardiac dysfunction (including cardiac failure, acute left ventricular failure, diastolic dysfunction, and ventricular hypertrophy) occurred in 1.7% of 351 patients, including Grade 3 adverse reactions in 1.1% of patients.

In INVICTUS, Grade 3 decreased ejection fraction occurred in 2.6% of the 77 patients who received QINLOCK and who had a baseline and at least one post-baseline echocardiogram. Grade 3 decreased ejection fraction occurred in 3.4% of the 263 patients in the pooled safety population who received QINLOCK and who had a baseline and at least one post-baseline echocardiogram.

In INVICTUS, cardiac dysfunction led to dose discontinuation in 1.2% of the 85 patients who received QINLOCK. The safety of QINLOCK has not been assessed in patients with a baseline ejection fraction below 50%. Assess ejection fraction by echocardiogram or MUGA scan prior to initiating QINLOCK and during treatment, as clinically indicated. Permanently discontinue QINLOCK for Grade 3 or 4 left ventricular systolic dysfunction.

Risk of Impaired Wound Healing: QINLOCK has the potential to adversely affect wound healing. Withhold QINLOCK for at least 1 week prior to elective surgery. Do not administer for at least 2 weeks following major surgery and until adequate wound healing. The safety of resumption of QINLOCK after resolution of wound healing complications has not been established.

Embryo-Fetal Toxicity: QINLOCK can cause fetal harm when administered to a pregnant woman. Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential and males with female partners of reproductive potential to use effective contraception during treatment and for at least 1 week after the final dose. Because of the potential for serious adverse reactions in the breastfed child, advise women not to breastfeed during treatment and for at least 1 week after the final dose. QINLOCK may impair fertility in males of reproductive potential.

Adverse Reactions: The most common adverse reactions (greater-than or equal to 20%) were alopecia, fatigue, nausea, abdominal pain, constipation, myalgia, diarrhea, decreased appetite, PPES, and vomiting. The most common Grade 3 or 4 laboratory abnormalities (greater-than or equal to 4%) were increased lipase and decreased phosphate.

The safety and effectiveness of QINLOCK in pediatric patients have not been established.

Administer strong CYP3A inhibitors with caution. Monitor patients who are administered strong CYP3A inhibitors more frequently for adverse reactions. Avoid concomitant use with strong CYP3A inducers.

Please click here to see the full U.S. Prescribing Information for QINLOCK.

About the INVICTUS Phase 3 Study

INVICTUS is a Phase 3 randomized, double-blind, placebo-controlled, international, multicenter clinical study evaluating the safety, tolerability, and efficacy of QINLOCK compared to placebo in patients with advanced GIST whose previous therapies have included imatinib, sunitinib, and regorafenib. Patients were randomized 2:1 to either 150 mg of QINLOCK or placebo once daily. The primary efficacy endpoint was progression-free survival (PFS) as determined by independent radiologic review using modified Response Evaluation Criteria in Solid Tumors (RECIST). The median PFS in the study was 6.3 months compared to 1.0 month in the placebo arm and significantly reduced the risk of disease progression or death by 85% (hazard ratio of 0.15, p<0.0001). Secondary endpoints as determined by independent radiologic review using modified RECIST include Objective Response Rate (ORR) and Overall Survival (OS). QINLOCK demonstrated an ORR of 9.4% compared with 0% for placebo (p =0.0504). QINLOCK also demonstrated a median OS of 15.1 months compared to 6.6 months in the placebo arm and reduced the risk of death by 64% (hazard ratio of 0.36).

About GIST

Gastrointestinal stromal tumor (GIST) is a cancer affecting the digestive tract or nearby structures within the abdomen, most often presenting in the stomach or small intestine. GIST is the most common sarcoma of the gastrointestinal tract, with approximately 4,000 to 6,000 new GIST cases each year in the United States and a similar incidence rate in European and other countries. Most cases of GIST are driven by a spectrum of mutations. The most common primary mutations are in KIT kinase, representing approximately 80% of cases, or in PDGFRA kinase, representing approximately 6% of cases. Current therapies are unable to inhibit the full spectrum of primary and secondary mutations, which drives resistance and disease progression. Estimates for 5-year survival range from 48% to 90%, depending on the stage of the disease at diagnosis. (Press release, Deciphera Pharmaceuticals, NOV 11, 2020, View Source [SID1234570584])

Calithera to Participate in Jefferies Virtual Healthcare Conference and SVB Leerink Oncology 1×1 Day

On November 11, 2020 Calithera Biosciences, Inc. (Nasdaq: CALA), a clinical-stage biotechnology company focused on discovering and developing novel small molecule drugs for the treatment of cancer and other life-threatening diseases, reported its participation at two upcoming healthcare investor conferences in November (Press release, Calithera Biosciences, NOV 11, 2020, View Source [SID1234570583]).

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Jefferies Virtual Healthcare Conference. Susan M. Molineaux, Ph.D., the company’s founder, president and chief executive officer will present on Wednesday, November 18, 2020, at 2:20 p.m. Eastern Time. The presentation will be webcast live and available for replay for up to 30 days at www.calithera.com in the Investor Relations section.
SVB Leerink Oncology 1×1 Day. The company will host virtual meetings with investors on Thursday, November 19, 2020.

HOOKIPA Pharma to Participate in Upcoming Investor Conferences in November

On November 11, 2020 HOOKIPA Pharma Inc. (NASDAQ: HOOK, ‘HOOKIPA’), a company developing a new class of immunotherapeutics based on its proprietary arenavirus platform, reported that HOOKIPA’s management team will participate in two upcoming virtual investor conferences (Press release, Hookipa Pharma, NOV 11, 2020, View Source [SID1234570582]):

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The SVB Leerink Oncology 1×1 Day, November 19, 2020
The Piper Sandler 32nd Annual Virtual Healthcare Conference, November 30 – December 3, 2020
HOOKIPA will participate in virtual one-on-one meetings during these events.

Deciphera Presents Updated Preliminary Data from DCC-3014, its CSF1R Inhibitor Program, in Tenosynovial Giant Cell Tumor Patients at the Connective Tissue Oncology Society (CTOS) 2020 Virtual Annual Meeting

On November 11, 2020 Deciphera Pharmaceuticals, Inc. (NASDAQ:DCPH), reported the presentation of encouraging preliminary results from the ongoing Phase 1/2 study of DCC-3014, a highly selective, oral, investigational switch-control kinase inhibitor of CSF1R, in patients with tenosynovial giant cell tumor (TGCT) (Press release, Deciphera Pharmaceuticals, NOV 11, 2020, View Source [SID1234570581]). The presentation, titled "Phase 1 Dose-Escalation Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of DCC-3014 in Advanced Solid Tumors and Tenosynovial Giant Cell Tumor (TGCT)", will be presented at the CTOS 2020 Virtual Annual Meeting, being held November 18-21, 2020. Posters and presentations are available to meeting participants as of November 11, 2020.

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"We are very encouraged by the updated data in additional TGCT patients from the ongoing Phase 1/2 study of DCC-3014," said Matthew L. Sherman, MD, Executive Vice President and Chief Medical Officer of Deciphera. "The preliminary results presented in TGCT patients at the CTOS 2020 Virtual Annual Meeting demonstrated highly encouraging evidence of anti-tumor activity, and DCC-3014 was shown to be generally well-tolerated. These results further support the evaluation of DCC-3014 in patients with TGCT and bolster our confidence in its potential to make a meaningful impact in this disease, which is typically associated with progressively reduced mobility and function. We have selected the recommended Phase 2 dose and initiated the TGCT expansion cohorts to further evaluate the safety and efficacy of DCC-3014."

"TGCT is a rare and debilitating disease that is most often treated with surgery," said William D. Tap, MD, Chief of the Sarcoma Medical Oncology Service at Memorial Sloan Kettering Cancer Center in New York. "Despite the best surgical intervention, the disease may advance to the point where surgery is no longer an option, and so there remains a need for effective, well-tolerated systemic therapies to help these patients. These preliminary results demonstrate that DCC-3014 has the potential to be a safe and effective treatment option for TGCT patients."

The Company’s international, multicenter, open-label Phase 1/2 study of DCC-3014 was designed to evaluate the safety, efficacy, pharmacokinetics, and pharmacodynamics of DCC-3014 in patients with malignant solid tumors and TGCT. Data presented at the CTOS 2020 Virtual Annual Meeting are from 25 TGCT patients enrolled in the dose-escalation portion of the Phase 1/2 study. The cutoff date for the safety data was September 23, 2020, and the cutoff date for the efficacy data was October 5, 2020.

Preliminary results from DCC-3014 in TGCT patients:

Dose Cohorts and Demographics

25 TGCT patients enrolled in the study in three dose cohorts:
Cohort 5 (n=7): 30 mg loading dose daily for five days followed by a maintenance dose of 30 mg twice a week;
Cohort 8 (n=12): 30 mg loading dose daily for three days followed by a maintenance dose of 10 mg daily; and
Cohort 9 (n=6): 20 mg loading dose daily for three days followed by a maintenance dose of 6 mg daily.
Seven patients (28%) had at least one prior surgery and four patients (16%) had received at least one prior systemic therapy.
Preliminary Efficacy and Duration of Treatment

22 patients were evaluable for efficacy by RECIST v1.1 at the data cutoff with central assessment available for 21 of the 22 patients; three patients had not yet reached first efficacy assessment.
Objective response rate of 41%.
Nine of 22 patients achieved an objective response, including one complete response.
Of the nine responses, three were confirmed and six are awaiting confirmation.
78% of responders (7 of 9 patients) had a partial response at their first restaging scan at Cycle 3 Day 1 (week 9).
22 of 25 patients were receiving treatment with DCC-3014 at the data cutoff. Two patients withdrew from the study and one patient discontinued due to an adverse event.
Two TGCT patients were on treatment for 12 or more months with responses that deepened over time.
Safety and Tolerability

Treatment with DCC-3014 was generally well-tolerated in patients with TGCT not amenable to surgery. One patient (4%) discontinued treatment due to an adverse event (asymptomatic Grade 3 AST elevation, from Grade 1 at baseline).
Treatment-emergent adverse events (TEAEs) (mostly grade 1/2) occurring in ≥25% of patients with TGCT regardless of relatedness were blood creatine phosphokinase (CPK) increased (52%), aspartate amino transferase (AST) increased (44%), periorbital edema (44%), fatigue (40%), lipase increased (32%), and alanine aminotransferase (ALT) increased (28%). No serious adverse events related to DCC-3014 were reported.
All bilirubin levels were within the normal limit.
Observed transaminase and pancreatic enzyme elevations were asymptomatic and not clinically significant.
Pharmacokinetics, Pharmacodynamics and Recommended Phase 2 Dose

Similar steady state pharmacokinetic profiles were observed between the 30 mg twice weekly (cohort 5) and 10 mg daily (cohort 8) dosing regimens; lower exposure was observed in the 6 mg daily (cohort 9) dosing regimen.
Across all cohorts, DCC-3014 treatment resulted in an increase in plasma CSF1/IL-34 and a decrease in non-classical sub-type of monocytes, indicating pharmacodynamic inhibition of CSF1R.
The recommended Phase 2 dose for DCC-3014 in TGCT patients was determined to be 30 mg twice weekly (no loading dose).
Based on these encouraging results, the Phase 1/2 study of DCC-3014 is ongoing and enrolling up to 60 patients into two expansion cohorts, one for TGCT patients with no prior exposure to anti-CSF1/CSF1R agents (n=40) and a second for patients with prior exposure to anti-CSF1/CSF1R agents (n=20). In addition, enrollment of an additional six patients in cohort 9 of the dose escalation portion of the study is ongoing to complete enrollment in this cohort.

About Tenosynovial Giant Cell Tumor (TGCT)
TGCT is a rare disease caused by a translocation in colony-stimulating factor 1 (CSF1) gene resulting in overexpression of CSF1 and recruitment of colony-stimulating factor 1 receptor (CSF1R)-positive inflammatory cells into the lesion. TGCT is also known as giant cell tumor of the tendon sheath (GCT-TS) or pigmented villonodular synovitis (PVNS), a diffuse-type of TGCT. Although benign, these tumors can grow and cause damage to surrounding tissues and structures inducing pain, swelling, and limitation of movement of the joint. Surgery is the main treatment option; however, these tumors tend to recur, particularly in diffuse-type TGCT. If untreated or if the tumor continually recurs, damage and degeneration may occur in the affected joint and surrounding tissues, which may cause significant disability.

About DCC-3014
DCC-3014 is an investigational, orally administered, potent and highly selective switch-control kinase inhibitor of CSF1R. DCC-3014 was designed using the Company’s proprietary discovery platform to selectively bind to the CSF1R switch pocket. Through inhibition of CSF1R, DCC-3014 has demonstrated encouraging preliminary efficacy and safety data in tenosynovial giant cell tumor (TGCT) and is currently being evaluated in a Phase 1/2 clinical study. For more information about the clinical trial design, please visit www.clinicaltrials.gov (NCT03069469).

Bio-Techne To Present At The Stephens Annual Investment Conference 2020

On November 11, 2020 Bio-Techne Corporation (NASDAQ: TECH) reported that Chuck Kummeth, President and Chief Executive Officer, will present at the Stephens Annual Investment Conference 2020 on Tuesday, November 17, 2020 at 3:00 p.m. EST (Press release, Bio-Techne, NOV 11, 2020, https://investors.bio-techne.com/news/detail/222/bio-techne-to-present-at-the-stephens-annual-investment-conference-2020 [SID1234570580]). A live webcast of the presentation can be accessed via the IR Calendar page of Bio-Techne’s Investor Relations website at View Source

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