Pilot Trial of XFBD, a TCM, in Persons With COVID-19

• ClinicalTrials.gov Identifier: NCT04810689
• Recruitment Status: Recruiting
• First Posted: March 23, 2021
• Last Update Posted: March 23, 2021
• Sponsor: Darcy Spicer
• Information provided by (Responsible Party): Darcy Spicer, University of Southern California

Study Description

Brief Summary:

The purpose of this study is to document the safety of taking traditional Chinese medicine (TCM) in patients with COVID-19 and to gain information to determine whether a study with TCM can be conducted. The study will test a traditional Chinese medicine that has been made into a granule formulation called Xuanfei Baidu Granules.

Condition or disease	Intervention/treatment	Phase
Covid19	Drug: Xuanfei Baidu Granules; Other: Placebo	Phase 2

Detailed Description:

Xuanfei Baidu granules (XFBD) is a 13 medicinal traditional Chinese medicine (TCM) prescription developed by Dr. Zhang Boli, a member of Chinese Academy of Engineering, and his team, and used in Wuhan, China, during the initial outbreak of SARS-CoV2. Based on TCM theory, the 13 medicinals used mainly consist of heat-clearing and toxin-removing medicinals to reduce fever and clear viruses; cough-suppressing and phlegm-transforming medicinals to thin and clear the phlegm; and lung-diffusing and pant-calming to soothe the tracheal smooth muscle and relieve shortness of breath. Another unique quality is one of the medicinals helps to dissipate stasis and dissolves blood clots, providing a mild anticoagulant effect.

Before the widespread usage of TCM, nationwide China saw a progression of disease of about 10% of their mild and moderate cases while during the period with the TCM utilization, the percentage dropped to 2-5% depending on the hospital. Overall, they saw an improvement of clinical symptoms. Due to the challenges of the rapidly evolving outbreak, these are clinical observations and not evidence from a controlled study.

The purpose of this initial pilot study is to document the safety of taking a TCM in patients with COVID-19 and to gain information to determine whether a study with TCM can be conducted in the US. The study will test a TCM which has been made into a granule formulation called XFBD.

This is a randomized double-blind placebo-control pilot trial to document safety and efficacy endpoint assessments and to determine the feasibility of community recruitment and enrollment of symptomatic adult outpatients with COVID-19. The 12-week pilot will have 14 days where they receive XFBD or a placebo, orally twice a day and a 10 week follow up. The study will have a total of 60 participants with approximately 30 participants in each treatment arm. The participants will be randomized 1:1 individuals.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 60 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Intervention Model Description: Study participants will be randomized to 1 of 2 arms: XFBD granules or placebo
• Masking: Triple (Participant, Investigator, Outcomes Assessor)
• Primary Purpose: Other
• Official Title: A Randomized, Double-Blind, Placebo-Control Pilot Trial of Xuanfei Baidu Granules (XFBD), a Traditional Chinese Medicine (TCM), in Persons With COVID-19
• Actual Study Start Date: March 1, 2021
• Estimated Primary Completion Date: March 1, 2022
• Estimated Study Completion Date: September 1, 2022

Arms and Interventions

Arm	Intervention/treatment
Experimental: XFBD Arm; XFBD (administered as 1 packet of granules dissolved in warm water) orally twice daily for 14 day, 1 hour after food in the morning and at night with at least 8 hours in between doses	Drug: Xuanfei Baidu Granules; Xuanfei Baidu granules is a prescription of 13 herbal medicinals made into dissolvable granules for oral intake; Other Name: XFBD
Placebo Comparator: Placebo Arm; Placebo (administered as 1 packet of granules dissolved in warm water) orally twice daily for 14 day, 1 hour after food in the morning and at night with at least 8 hours in between doses	Other: Placebo; Placebo for Xuanfei Baidu granule made into dissolvable granules for oral intake

Outcome Measures

Primary Outcome Measures :

1. Feasibility of recruitment [ Time Frame: 90 days ]
   To document the feasibility of recruitment through community setting by assessment of the number of positive cases identified per week
2. Participation Rate [ Time Frame: 90 days ]
   To document the proportion of patients who agree to participate as measured by enrollment and randomization.
3. Side Effects and Safety Profile [ Time Frame: up to 90 days after enrollment ]
   To document the treatment emergent side effects and safety profile of the XFBD and placebo
4. Rate of hospitalization or death [ Time Frame: up to 42 days after enrollment ]
   To document the rate of hospitalization or death within 42 days of enrollment in the XFBD and placebo treated groups.

Secondary Outcome Measures :

1. Symptom Severity Score [ Time Frame: up to 28 days after enrollment ]
   To document the effect of XFBD on Symptom Severity Score within 28 days of enrollment in the XFBD and placebo treatment.
2. Study agent compliance [ Time Frame: up to 14 days after enrollment ]
   To document the proportion of patients who are compliant taking greater than 90% of the test substance as measured by self-report
3. Symptom monitoring compliance [ Time Frame: up to 90 days after enrollment ]
   To document the proportion of patients who comply with symptom monitoring.
4. COVID-19 testing compliance [ Time Frame: up to 14 days after enrollment ]
   To document the proportion of patients who comply with repeated clinical testing.
5. Hospital-free days [ Time Frame: up to 42 days after enrollment ]
   To document the hospital-free days from enrollment to 42 days (number of days patient not in hospital)
6. Adverse Events [ Time Frame: up to 14 days after enrollment ]
   To document cumulative incidence of serious adverse events, and adverse events leading to early discontinuation of XFBD or placebo.
7. Grade 3 and 4 adverse events [ Time Frame: up to 28 days after enrollment ]
   To document cumulative incidence of grade 3 and 4 adverse events
8. Viral load [ Time Frame: up to 14 days after enrollment ]
   To obtain levels (detectable versus not detectable, and continuous on log10 scale) of SARS-CoV-2 RNA from nasal swabs at approximately days 1, 7 and 14 among a subset

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 75 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Participant provides informed consent prior to initiation of any study procedures.
• Individual 18 to 75 years of age.
• Documentation of confirmed active SARS-CoV-2 infection, as determined by an FDA authorized molecular test conducted at any US clinic or laboratory that has a Clinical Laboratory Improvement Amendments (CLIA) certification or its equivalent from any respiratory specimen collected <96 hours prior to study entry.

• Mild or Moderate COVID-19 experiencing at least one SARS-CoV-2 infection symptom including:

  • Mild Covid-19: Symptoms of mild illness with COVID-19 that could include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, without shortness of breath or dyspnea

  • Moderate Covid-19:

    • Symptoms of moderate illness with COVID-19, which could include any symptom of mild illness or shortness of breath with exertion
    • Presence of clinical signs consistent with moderate illness with COVID-19, such as respiratory rate ≥ 20 breaths per minute, saturation of oxygen (SpO2) > 93% on room air at sea level, heart rate ≥ 90 beats per minute from a health care encounter within 48 hours.
• Agrees to not participate in another clinical trial for the treatment of COVID-19 or SARS-CoV-2 during the study period up until reaching hospitalization or 28 days, whichever is earliest.
• Agrees to not utilize TCM outside of this study.
• Willing to be randomized to XFBD and placebo control arm for 14 days, and followed up to 12 weeks.
• Willing to comply with the study related questionnaires, procedures and measurements.
• Will to not become pregnant during the 14 days of test substance ingestion using appropriate accepted methods of contraception. Acceptable methods of contraception include: postmenopausal 1 year of amenorrhea and over 50 years of age; prior tubal ligation or hysterectomy; or barrier contraception using condom or diaphragm plus spermicide.
• Able to provide the identity of their health care provider or health system clinical care entry information.
• Able to utilize telephone and telehealth platform to comply with the study related questionnaires, procedures and measurements. Established during the recruitment process.
• Able to speak and communicate in English, Spanish, Mandarin Chinese or Cantonese.

Exclusion Criteria:

• Need for hospitalization.

• Severe or Critical COVID-19:

  • Severe COVID-19

    • Symptoms suggestive of severe systemic illness with COVID-19, which could include any symptom of moderate illness or shortness of breath at rest, or respiratory distress
    • Clinical signs indicative of severe systemic illness with COVID-19, respiratory rate ≥ 30 breaths per minute, heart rate ≥ 125 beats per minute, SpO2 ≤ 93% on room air at sea level or respiratory PaO2/FiO2 < 300

  • Critical COVID-19 -- Evidence of critical illness, defined by at least one of the following:

    • Respiratory failure defined based on resource utilization requiring at least one of the following: Endotracheal intubation and mechanical ventilation, oxygen delivered by high flow nasal cannula (heated, humidified, oxygen delivered via reinforced nasal cannula at flow rates > 20 L/min with fraction of delivered oxygen ≥ 0.5), noninvasive positive pressure ventilation, ECMO, or clinical diagnosis of respiratory failure (i.e., clinical need for one of the preceding therapies, but preceding therapies not able to be administered in setting of resource limitation)
    • Shock (defined by systolic blood pressure < 90 mm Hg, or diastolic blood pressure < 60 mm Hg or requiring vasopressors)
    • Multi-organ dysfunction/failure
• Positive SARS-CoV-2 molecular test in the absence of Covid-19 symptoms. However if patients develop symptoms within 14 days of the positive test and fulfill all other enrollment criteria, they are eligible for participation.
• Receiving the following classes of agents found in 5.4.1. Prohibited Medications
• Use of drugs for anti-SARS-CoV-2 treatment including remdesivir, baricitinib, lopinavir/ritonavir fixed dose combination, ribavirin, chloroquine, hydroxychloroquine, and azithromycin, dexamethasone, bamlanivimab, casirivimab plus imdevimab convalescent plasma, or participation in a clinical trial involving any of these drugs whether for treatment or prophylaxis.
• Participating in a study where co-enrollment is not allowed.
• Receipt of a SARS-CoV-2 vaccination prior to study entry.
• Known allergy/sensitivity or any hypersensitivity to components of XFBD
• Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.
• Has known prior kidney disease.
• Has known cirrhosis, acute liver disease or uncontrolled chronic liver disease.
• Has known severe coronary artery disease.
• Has known narrow angle glaucoma.
• Has greater than two or a single uncontrolled underlying comorbid condition including cardiovascular disease (coronary artery disease, heart failure, valvular heart disease), hypertension, diabetes, chronic lung disease, chronic kidney disease, chronic liver disease, immunocompromised (HIV or daily users of more than 5 mg/day of prednisone), prior organ transplant.
• Fulfills the FDA EUA criteria of at high risk for progressing to severe COVID-19. This includes high-risk individuals specified in the EUA who meet at least one of the following criteria: Body mass index (BMI) ≥35; Chronic kidney disease; Diabetes mellitus; Immunocompromising condition/immunosuppressive disease; Currently receiving immunosuppressive treatment; Aged ≥65 years; or Aged ≥55 years and have: Cardiovascular disease, or Hypertension, or Chronic obstructive pulmonary disease/other chronic respiratory disease. If the patient is not able to receive the EUA agent casirivimab and imdevimab (Regeneron) or bamlanivimab (Eli Lilly) because of unavailability this exclusion may be waived.
• Women who are currently pregnant or breastfeeding.

Contacts and Locations

Contacts

Contact: Darcy V Spicer, MD; 3238653904; dspicer@usc.edu

Contact: Elizabeth Qi, PharmD; eqi@usc.edu

Locations

United States, California

University of Southern California; Recruiting

Los Angeles, California, United States, 90033

Principal Investigator: Darcy Spicer, MD

Sub-Investigator: Peter Kuhn, PhD

Sub-Investigator: Anna Wu, PhD

Sub-Investigator: Ann Hamilton, PhD

Sub-Investigator: Cheryl Vigen, PhD

Sub-Investigator: Elizabeth Qi, PharmD

Sponsors and Collaborators

Darcy Spicer

Investigators

• Principal Investigator: Darcy V Spicer, MD; Keck Medicine of USC

More Information

• Responsible Party: Darcy Spicer, Associate Professor, University of Southern California
• ClinicalTrials.gov Identifier: NCT04810689
• Other Study ID Numbers: HS-20-00632
• First Posted: March 23, 2021
• Last Update Posted: March 23, 2021
• Last Verified: March 2021

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Darcy Spicer, University of Southern California:

Covid19

Additional relevant MeSH terms:

COVID-19; Respiratory Tract Infections; Infections; Pneumonia, Viral; Pneumonia; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases